General Information of Drug (ID: DMJPBAX)

Drug Name
Oxybutynine
Synonyms
5633-20-5; Ditropan; Oxytrol; Oxibutyninum; Oxybutyninum; Oxibutinina; Oxybutyninum [INN-Latin]; Oxybutynine [INN-French]; Oxybutinin; Cystrin; Oxibutinina [INN-Spanish]; Oxybutynin Base; transdermal patch; Lyrinel XL; Oxybutynin [USAN:INN:BAN]; 4-Diethylamino-2-butinyl alpha-cyclohexylmandelat; CCRIS 1923; oxybutynin topical gel; Ditropan Xl; Oxybutynin (Ditropan); HSDB 3270; 4-Diethylamino-2-butynyl alpha-phenylcyclohexaneglycolate; CHEMBL1231; Cyclohexaneglycolic acid, alpha-phenyl-, 4-(diethylamino)-2-b
Indication
Disease Entry ICD 11 Status REF
Obsolete neurogenic bladder N.A. Approved [1]
Discovery agent N.A. Investigative [2]
Priapism N.A. Investigative [1]
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 357.5
Logarithm of the Partition Coefficient (xlogp) 4.2
Rotatable Bond Count (rotbonds) 8
Hydrogen Bond Donor Count (hbonddonor) 1
Hydrogen Bond Acceptor Count (hbondacc) 4
ADMET Property
Absorption Tmax
The time to maximum plasma concentration (Tmax) is 45 min-2.25 h []
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [3]
Bioavailability
The bioavailability of drug is 94% []
Clearance
The drug present in the plasma can be removed from the body at the rate of 5.1 mL/min/kg [4]
Elimination
Oxybutynin is heavily cleared by the liver, and less than 0.1% of an administered dose is found as unchanged drug in the urine [5]
Half-life
The concentration or amount of drug in body reduced by one-half in 2 hours [6]
Metabolism
The drug is metabolized via the CYP3A4 enzyme system in both the liver and the wall of the intestine [7]
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 0.93148 micromolar/kg/day [8]
Unbound Fraction
The unbound fraction of drug in plasma is 0.0034% [4]
Vd
The volume of distribution (Vd) of drug is 193 L [9]
Water Solubility
The ability of drug to dissolve in water is measured as 0.8 mg/mL [3]
Chemical Identifiers
Formula
C22H31NO3
IUPAC Name
4-(diethylamino)but-2-ynyl 2-cyclohexyl-2-hydroxy-2-phenylacetate
Canonical SMILES
CCN(CC)CC#CCOC(=O)C(C1CCCCC1)(C2=CC=CC=C2)O
InChI
InChI=1S/C22H31NO3/c1-3-23(4-2)17-11-12-18-26-21(24)22(25,19-13-7-5-8-14-19)20-15-9-6-10-16-20/h5,7-8,13-14,20,25H,3-4,6,9-10,15-18H2,1-2H3
InChIKey
XIQVNETUBQGFHX-UHFFFAOYSA-N
Cross-matching ID
PubChem CID
4634
ChEBI ID
CHEBI:7856
CAS Number
5633-20-5
DrugBank ID
DB01062
TTD ID
D0F5LH
ACDINA ID
D00501
Repurposed Drugs (RPD) Click to Jump to the Detailed RPD Information of This Drug

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Muscarinic acetylcholine receptor M3 (CHRM3) TTQ13Z5 ACM3_HUMAN Antagonist [2]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Antileukoproteinase (SLPI) OTUNFUU8 SLPI_HUMAN Gene/Protein Processing [10]
Bile salt export pump (ABCB11) OTRU7THO ABCBB_HUMAN Gene/Protein Processing [11]
Cocaine esterase (CES2) OTC647SQ EST2_HUMAN Biotransformations [12]
Cytochrome P450 2C8 (CYP2C8) OTHCWT42 CP2C8_HUMAN Gene/Protein Processing [13]
Hepatocyte growth factor receptor (MET) OT7K55MU MET_HUMAN Gene/Protein Processing [10]
Interleukin-24 (IL24) OT4VUWH1 IL24_HUMAN Gene/Protein Processing [10]
Phosphatidylcholine translocator ABCB4 (ABCB4) OTE6PY83 MDR3_HUMAN Gene/Protein Processing [14]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Molecular Expression Atlas of This Drug

The Studied Disease Obsolete neurogenic bladder
ICD Disease Classification
Molecule Name Molecule Type Gene Name p-value Fold-Change Z-score
Muscarinic acetylcholine receptor M3 (CHRM3) DTT CHRM3 4.61E-07 -0.59 -0.73
Molecular Expression Atlas (MEA) Jump to Detail Molecular Expression Atlas of This Drug

Drug-Drug Interaction (DDI) Information of This Drug

Coadministration of a Drug Treating the Disease Different from Oxybutynine (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Arn-509 DMT81LZ Moderate Increased metabolism of Oxybutynine caused by Arn-509 mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [15]
Oliceridine DM6MDCF Moderate Additive CNS depression effects by the combination of Oxybutynine and Oliceridine. Acute pain [MG31] [16]
Mepyramine DMB4SFH Moderate Additive anticholinergic effects by the combination of Oxybutynine and Mepyramine. Allergic/hypersensitivity disorder [4A80-4A8Z] [17]
Phenyltoloxamine DMKAEQW Moderate Additive anticholinergic effects by the combination of Oxybutynine and Phenyltoloxamine. Allergic/hypersensitivity disorder [4A80-4A8Z] [17]
Desipramine DMT2FDC Moderate Additive anticholinergic effects by the combination of Oxybutynine and Desipramine. Attention deficit hyperactivity disorder [6A05] [18]
Cariprazine DMJYDVK Moderate Additive anticholinergic effects by the combination of Oxybutynine and Cariprazine. Bipolar disorder [6A60] [18]
Tucatinib DMBESUA Moderate Decreased metabolism of Oxybutynine caused by Tucatinib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [19]
Acetylcholine DMDF79Z Moderate Antagonize the effect of Oxybutynine when combined with Acetylcholine. Cataract [9B10] [20]
Umeclidinium DM4E8O9 Moderate Additive anticholinergic effects by the combination of Oxybutynine and Umeclidinium. Chronic obstructive pulmonary disease [CA22] [21]
Tiotropium DMFDC0Q Moderate Additive anticholinergic effects by the combination of Oxybutynine and Tiotropium. Chronic obstructive pulmonary disease [CA22] [21]
Revefenacin DMMP5SI Moderate Additive anticholinergic effects by the combination of Oxybutynine and Revefenacin. Chronic obstructive pulmonary disease [CA22] [21]
Dihydrocodeine DMB0FWL Moderate Additive CNS depression effects by the combination of Oxybutynine and Dihydrocodeine. Chronic pain [MG30] [22]
Arbutamine DMCY8AF Moderate Increased risk of rapid heart rate by the combination of Oxybutynine and Arbutamine. Coronary atherosclerosis [BA80] [23]
MK-8228 DMOB58Q Moderate Decreased metabolism of Oxybutynine caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [24]
OPC-34712 DMHG57U Moderate Additive anticholinergic effects by the combination of Oxybutynine and OPC-34712. Depression [6A70-6A7Z] [18]
Clomipramine DMINRKW Moderate Additive anticholinergic effects by the combination of Oxybutynine and Clomipramine. Depression [6A70-6A7Z] [18]
Doxepin DMPI98T Moderate Additive anticholinergic effects by the combination of Oxybutynine and Doxepin. Depression [6A70-6A7Z] [17]
Mepenzolate DM8YU2F Moderate Additive anticholinergic effects by the combination of Oxybutynine and Mepenzolate. Digestive system disease [DE2Z] [18]
Cenobamate DM8KLU9 Moderate Increased metabolism of Oxybutynine caused by Cenobamate mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [25]
Stiripentol DMMSDOY Moderate Decreased metabolism of Oxybutynine caused by Stiripentol mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [26]
Rufinamide DMWE60C Moderate Increased metabolism of Oxybutynine caused by Rufinamide mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [15]
Diphenhydramine DMKQTBA Moderate Additive anticholinergic effects by the combination of Oxybutynine and Diphenhydramine. Episodic vestibular syndrome [AB31] [18]
Nadolol DMW6GVL Moderate Antagonize the effect of Oxybutynine when combined with Nadolol. Essential hypertension [BA00] [15]
Tazemetostat DMWP1BH Moderate Increased metabolism of Oxybutynine caused by Tazemetostat mediated induction of CYP450 enzyme. Follicular lymphoma [2A80] [27]
Solifenacin DMG592Q Moderate Additive anticholinergic effects by the combination of Oxybutynine and Solifenacin. Functional bladder disorder [GC50] [18]
Pilocarpine DMV9ADG Moderate Antagonize the effect of Oxybutynine when combined with Pilocarpine. Glaucoma [9C61] [28]
Carvedilol DMHTEAO Moderate Antagonize the effect of Oxybutynine when combined with Carvedilol. Heart failure [BD10-BD1Z] [15]
Boceprevir DMBSHMF Moderate Decreased metabolism of Oxybutynine caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [29]
Telaprevir DMMRV29 Moderate Decreased metabolism of Oxybutynine caused by Telaprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [30]
Rifapentine DMCHV4I Moderate Increased metabolism of Oxybutynine caused by Rifapentine mediated induction of CYP450 enzyme. HIV-infected patients with tuberculosis [1B10-1B14] [31]
Etravirine DMGV8QU Moderate Increased metabolism of Oxybutynine caused by Etravirine mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [32]
Darunavir DMN3GCH Moderate Decreased metabolism of Oxybutynine caused by Darunavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [33]
Acebutolol DM0TI4U Moderate Antagonize the effect of Oxybutynine when combined with Acebutolol. Hypertension [BA00-BA04] [15]
Penbutolol DM4ES8F Moderate Antagonize the effect of Oxybutynine when combined with Penbutolol. Hypertension [BA00-BA04] [15]
Nebivolol DM7F1PA Moderate Antagonize the effect of Oxybutynine when combined with Nebivolol. Hypertension [BA00-BA04] [15]
Belladonna DM2RBWK Moderate Additive anticholinergic effects by the combination of Oxybutynine and Belladonna. Infectious gastroenteritis/colitis [1A40] [18]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Oxybutynine caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [34]
ITI-007 DMUQ1DO Moderate Additive anticholinergic effects by the combination of Oxybutynine and ITI-007. Insomnia [7A00-7A0Z] [18]
R0-93877 DMM4U9G Moderate Antagonize the effect of Oxybutynine when combined with R0-93877. Irritable bowel syndrome [DD91] [26]
Brigatinib DM7W94S Moderate Increased metabolism of Oxybutynine caused by Brigatinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [35]
PF-06463922 DMKM7EW Moderate Increased metabolism of Oxybutynine caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [36]
Selpercatinib DMZR15V Moderate Decreased metabolism of Oxybutynine caused by Selpercatinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [15]
Idelalisib DM602WT Moderate Decreased metabolism of Oxybutynine caused by Idelalisib mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [37]
IPI-145 DMWA24P Moderate Decreased metabolism of Oxybutynine caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [38]
Dabrafenib DMX6OE3 Moderate Increased metabolism of Oxybutynine caused by Dabrafenib mediated induction of CYP450 enzyme. Melanoma [2C30] [15]
Exjade DMHPRWG Moderate Decreased metabolism of Oxybutynine caused by Exjade mediated inhibition of CYP450 enzyme. Mineral absorption/transport disorder [5C64] [39]
Neostigmine DM6T2J3 Moderate Antagonize the effect of Oxybutynine when combined with Neostigmine. Myasthenia gravis [8C6Y] [40]
Ambenonium DMOP0BL Moderate Antagonize the effect of Oxybutynine when combined with Ambenonium. Myasthenia gravis [8C6Y] [40]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Oxybutynine caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [15]
Nilotinib DM7HXWT Moderate Decreased metabolism of Oxybutynine caused by Nilotinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [41]
Dasatinib DMJV2EK Moderate Decreased metabolism of Oxybutynine caused by Dasatinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [42]
Phenindamine DMDTC7R Moderate Additive anticholinergic effects by the combination of Oxybutynine and Phenindamine. Nasopharyngitis [CA00] [18]
Promethazine DM6I5GR Moderate Additive anticholinergic effects by the combination of Oxybutynine and Promethazine. Nausea/vomiting [MD90] [18]
Cyclizine DM9G7BS Moderate Additive anticholinergic effects by the combination of Oxybutynine and Cyclizine. Nausea/vomiting [MD90] [18]
Metoclopramide DMFA5MY Moderate Antagonize the effect of Oxybutynine when combined with Metoclopramide. Nausea/vomiting [MD90] [43]
Polythiazide DMCH80F Minor Altered absorption of Oxybutynine due to GI dynamics variation caused by Polythiazide. Oedema [MG29] [44]
Levomethadyl Acetate DM06HG5 Moderate Additive CNS depression effects by the combination of Oxybutynine and Levomethadyl Acetate. Opioid use disorder [6C43] [22]
Rucaparib DM9PVX8 Moderate Decreased metabolism of Oxybutynine caused by Rucaparib mediated inhibition of CYP450 enzyme. Ovarian cancer [2C73] [45]
Oxymorphone DM65AGJ Moderate Additive CNS depression effects by the combination of Oxybutynine and Oxymorphone. Pain [MG30-MG3Z] [16]
Dezocine DMJDB0Y Moderate Additive CNS depression effects by the combination of Oxybutynine and Dezocine. Pain [MG30-MG3Z] [16]
Flavoxate DMKV4NL Moderate Additive anticholinergic effects by the combination of Oxybutynine and Flavoxate. Pain [MG30-MG3Z] [18]
Levodopa DMN3E57 Moderate Altered absorption of Oxybutynine due to GI dynamics variation caused by Levodopa. Parkinsonism [8A00] [46]
Orphenadrine DMW542E Moderate Additive anticholinergic effects by the combination of Oxybutynine and Orphenadrine. Parkinsonism [8A00] [18]
Abametapir DM2RX0I Moderate Decreased metabolism of Oxybutynine caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [47]
Methylscopolamine DM5VWOB Moderate Additive anticholinergic effects by the combination of Oxybutynine and Methylscopolamine. Peptic ulcer [DA61] [18]
Lefamulin DME6G97 Moderate Decreased metabolism of Oxybutynine caused by Lefamulin mediated inhibition of CYP450 enzyme. Pneumonia [CA40] [48]
Lonafarnib DMGM2Z6 Moderate Decreased metabolism of Oxybutynine caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [49]
Enzalutamide DMGL19D Moderate Increased metabolism of Oxybutynine caused by Enzalutamide mediated induction of CYP450 enzyme. Prostate cancer [2C82] [50]
Levomepromazine DMIKFEL Moderate Additive anticholinergic effects by the combination of Oxybutynine and Levomepromazine. Psychotic disorder [6A20-6A25] [18]
Quetiapine DM1N62C Moderate Additive anticholinergic effects by the combination of Oxybutynine and Quetiapine. Schizophrenia [6A20] [18]
Aripiprazole DM3NUMH Moderate Additive anticholinergic effects by the combination of Oxybutynine and Aripiprazole. Schizophrenia [6A20] [18]
Iloperidone DM6AUFY Moderate Additive anticholinergic effects by the combination of Oxybutynine and Iloperidone. Schizophrenia [6A20] [18]
Paliperidone DM7NPJS Moderate Additive anticholinergic effects by the combination of Oxybutynine and Paliperidone. Schizophrenia [6A20] [18]
Molindone DMAH70G Moderate Additive anticholinergic effects by the combination of Oxybutynine and Molindone. Schizophrenia [6A20] [18]
Thiothixene DMDINC4 Moderate Additive anticholinergic effects by the combination of Oxybutynine and Thiothixene. Schizophrenia [6A20] [18]
Asenapine DMSQZE2 Moderate Additive anticholinergic effects by the combination of Oxybutynine and Asenapine. Schizophrenia [6A20] [18]
Pimozide DMW83TP Moderate Additive anticholinergic effects by the combination of Oxybutynine and Pimozide. Schizophrenia [6A20] [18]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Oxybutynine caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [51]
Telotristat ethyl DMDIYFZ Moderate Increased metabolism of Oxybutynine caused by Telotristat ethyl mediated induction of CYP450 enzyme. Small intestine developmental anomaly [DA90] [15]
Larotrectinib DM26CQR Moderate Decreased metabolism of Oxybutynine caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [52]
Armodafinil DMGB035 Minor Increased metabolism of Oxybutynine caused by Armodafinil mediated induction of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [53]
LEE011 DMMX75K Moderate Decreased metabolism of Oxybutynine caused by LEE011 mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [54]
Pitolisant DM8RFNJ Moderate Increased metabolism of Oxybutynine caused by Pitolisant mediated induction of CYP450 enzyme. Somnolence [MG42] [15]
Fostamatinib DM6AUHV Moderate Decreased metabolism of Oxybutynine caused by Fostamatinib mediated inhibition of CYP450 enzyme. Thrombocytopenia [3B64] [55]
Pramlintide DM0EZ9Q Moderate Altered absorption of Oxybutynine due to GI dynamics variation caused by Pramlintide. Type-1/2 diabete [5A10-5A11] [56]
Chlorpheniramine DM5URA2 Moderate Additive anticholinergic effects by the combination of Oxybutynine and Chlorpheniramine. Vasomotor/allergic rhinitis [CA08] [18]
Trimeprazine DMEMV9D Moderate Additive anticholinergic effects by the combination of Oxybutynine and Trimeprazine. Vasomotor/allergic rhinitis [CA08] [17]
Acrivastine DMTIGA0 Moderate Additive anticholinergic effects by the combination of Oxybutynine and Acrivastine. Vasomotor/allergic rhinitis [CA08] [18]
⏷ Show the Full List of 88 DDI Information of This Drug

Drug Inactive Ingredient(s) (DIG) and Formulation(s) of This Drug

DIG
DIG Name DIG ID PubChem CID Functional Classification
Acrylic acid E00132 6581 Other agent
Allura red AC dye E00338 33258 Colorant
Butylated hydroxytoluene E00336 31404 Antioxidant
D&C red no. 27 E00381 83511 Colorant
FD&C blue no. 1 E00263 19700 Colorant
FD&C blue no. 2 E00446 2723854 Colorant
Isopropyl alcohol E00070 3776 Antimicrobial preservative; Solvent
Kyselina citronova E00014 311 Acidulant; Antioxidant; Buffering agent; Complexing agent; Flavoring agent
Mannitol E00103 6251 Diluent; Flavoring agent; Lyophilization aid; Plasticizing agent; Tonicity agent
methylparaben E00149 7456 Antimicrobial preservative
Quinoline yellow WS E00309 24671 Colorant
Sodium citrate anhydrous E00102 6224 Alkalizing agent; Buffering agent; Complexing agent; Emulsifying agent
Sodium lauryl sulfate E00464 3423265 Emulsifying agent; Modified-release agent; Penetration agent; Solubilizing agent; Surfactant; lubricant
Sunset yellow FCF E00255 17730 Colorant
Food blue 1 aluminum lake E00512 11979396 Colorant
Beta-D-lactose E00099 6134 Diluent; Dry powder inhaler carrier; Lyophilization aid
Calcium hydrogenphosphate E00294 24441 Diluent
Calcium stearate E00244 15324 lubricant
Carmellose sodium E00625 Not Available Disintegrant
Dextrose anhydrous E00394 107526 Binding agent; Diluent; Flavoring agent; Tonicity agent
Eisenoxyd E00585 56841934 Colorant
Ferric hydroxide oxide yellow E00539 23320441 Colorant
Ferrosoferric oxide E00231 14789 Colorant
Glycerin E00026 753 Antimicrobial preservative; Emollient; Flavoring agent; Humectant; Lubricant; Plasticizing agent; Solvent; Suppository base; Tonicity agent; Viscosity-controlling agent
Hypromellose E00634 Not Available Coating agent
Lactose monohydrate E00393 104938 Binding agent; Diluent; Dry powder inhaler carrier; Lyophilization aid
Magnesium stearate E00208 11177 lubricant
Polyethylene glycol 3350 E00652 Not Available Coating agent; Diluent; Ointment base; Plasticizing agent; Solvent; Suppository base; lubricant
Polyethylene glycol 400 E00653 Not Available Coating agent; Diluent; Ointment base; Plasticizing agent; Solvent; Suppository base; lubricant
Polyethylene glycol 4000 E00654 Not Available Coating agent; Diluent; Ointment base; Plasticizing agent; Solvent; Suppository base; lubricant
Polysorbate 80 E00665 Not Available Dispersing agent; Emollient; Emulsifying agent; Plasticizing agent; Solubilizing agent; Surfactant; Suspending agent
Povidone E00667 Not Available Binding agent; Coating agent; Disintegrant; Film/membrane-forming agent; Solubilizing agent; Suspending agent
Propylene glycol E00040 1030 Antimicrobial preservative; Humectant; Plasticizing agent; Solvent
Saccharose E00091 5988 Binding agent; Coating agent; Cryoprotectant; Diluent; Flavoring agent; Suspending agent; Viscosity-controlling agent
Silicon dioxide E00670 Not Available Anticaking agent; Opacifying agent; Viscosity-controlling agent
Sodium bicarbonate E00424 516892 Alkalizing agent; Diluent
Sodium chloride E00077 5234 Diluent; Tonicity agent
Sodium hydroxide E00234 14798 Alkalizing agent
Talc E00520 16211421 Anticaking agent; Diluent; Glidant; lubricant
Tartaric acid E00029 875 Acidulant; Complexing agent; Flavoring agent
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
Triacetin E00080 5541 Humectant; Plasticizing agent; Solvent
Triethyl citrate E00128 6506 Plasticizing agent; Solvent
Water E00035 962 Solvent
FD&C Green 3 E00682 16887 Colorant
Haematite red E00236 14833 Colorant
Sorbitan tristearate E00516 17800859 Dispersing agent; Emulsifying agent; Solubilizing agent; Surfactant; Suspending agent; Vaccine adjuvant
Cellulose acetate E00702 Not Available Coating agent; Modified-release agent; Diluent
Cellulose microcrystalline E00698 Not Available Adsorbent; Suspending agent; Diluent
⏷ Show the Full List of 49 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Oxybutynin 10 mg tablet 10 mg 24 HR Extended Release Oral Tablet Oral
Oxybutynin 15 mg tablet 15 mg 24 HR Extended Release Oral Tablet Oral
Oxybutynin 5 mg tablet 5 mg 24 HR Extended Release Oral Tablet Oral
Oxybutynin 5mg extended release tablet 5mg Extended Release Tablet Oral
Oxybutynin 5mg/5ml Syrup 5mg/5ml Syrup Oral
Oxybutynin 5 mg tablet 5 mg Oral Tablet Oral
Oxybutynin 5mg tablet 5mg Tablet Oral
Oxybutynin 3.9mg extended release film 3.9mg Extended Release Film Transdermal
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

1 A standard database for drug repositioning. Sci Data. 2017 Mar 14;4:170029.
2 Generation of an agonistic binding site for blockers of the M(3) muscarinic acetylcholine receptor. Biochem J. 2008 May 15;412(1):103-12.
3 BDDCS applied to over 900 drugs
4 Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 1352 Drug Compounds
5 Douchamps J, Derenne F, Stockis A, Gangji D, Juvent M, Herchuelz A: The pharmacokinetics of oxybutynin in man. Eur J Clin Pharmacol. 1988;35(5):515-20. doi: 10.1007/bf00558247.
6 A comparative review of oxybutynin chloride formulations: pharmacokinetics and therapeutic efficacy in overactive bladder. Rev Urol. 2010 Winter;12(1):12-9.
7 Legrand E: Aceclofenac in the management of inflammatory pain. Expert Opin Pharmacother. 2004 Jun;5(6):1347-57.
8 Estimating the safe starting dose in phase I clinical trials and no observed effect level based on QSAR modeling of the human maximum recommended daily dose
9 Ditropan XL FDA label
10 An in vitro coculture system of human peripheral blood mononuclear cells with hepatocellular carcinoma-derived cells for predicting drug-induced liver injury. Arch Toxicol. 2021 Jan;95(1):149-168. doi: 10.1007/s00204-020-02882-4. Epub 2020 Aug 20.
11 Interference with bile salt export pump function is a susceptibility factor for human liver injury in drug development. Toxicol Sci. 2010 Dec; 118(2):485-500.
12 Hydrolytic profile for ester- or amide-linkage by carboxylesterases pI 5.3 and 4.5 from human liver. Biol Pharm Bull. 1997 Aug;20(8):869-73. doi: 10.1248/bpb.20.869.
13 Examination of 209 drugs for inhibition of cytochrome P450 2C8. J Clin Pharmacol. 2005 Jan;45(1):68-78.
14 Evaluating the Role of Multidrug Resistance Protein 3 (MDR3) Inhibition in Predicting Drug-Induced Liver Injury Using 125 Pharmaceuticals. Chem Res Toxicol. 2017 May 15;30(5):1219-1229. doi: 10.1021/acs.chemrestox.7b00048. Epub 2017 May 4.
15 Cerner Multum, Inc. "UK Summary of Product Characteristics.".
16 Product Information. Apadaz (acetaminophen-benzhydrocodone). KemPharm, Inc, Coralville, IA.
17 Kulik AV, Wilbur R "Delirium and stereotypy from anticholinergic antiparkinson drugs." Prog Neuropsychopharmacol Biol Psychiatry 6 (1982): 75-82. [PMID: 7202232]
18 Cohen MA, Alfonso CA, Mosquera M. Development of urinary retention during treatment with clozapine and meclizine [published correction appears in Am J Psychiatry 1994 Jun;151(6):952]. Am J Psychiatry. 1994;151(4):619-620. [PMID: 8147469]
19 Product Information. Tukysa (tucatinib). Seattle Genetics Inc, Bothell, WA.
20 Multum Information Services, Inc. Expert Review Panel.
21 Cole JM, Sheehan AH, Jordan JK "Concomitant use of ipratropium and tiotropium in chronic obstructive plmonary disease." Ann Pharmacother 46 (2012): 1717-21. [PMID: 23170031]
22 Product Information. Exalgo (hydromorphone). Covidien, Mansfield, MA.
23 Product Information. GenESA (arbutamine). Gensia Inc, San Diego, CA.
24 Product Information. Prevymis (letermovir). Merck & Company Inc, Whitehouse Station, NJ.
25 Product Information. Xcopri (cenobamate). SK Life Science, Inc., Paramus, NJ.
26 EMEA. European Medicines Agency "EPARs. European Union Public Assessment Reports.".
27 Product Information. Tazverik (tazemetostat). Epizyme, Inc, Cambridge, MA.
28 Benjamin KW "Toxicity of ocular medications." Int Ophthalmol Clin 19 (1979): 199-255. [PMID: 376469]
29 Product Information. Victrelis (boceprevir). Schering-Plough Corporation, Kenilworth, NJ.
30 Product Information. Incivek (telaprevir). Vertex Pharmaceuticals, Cambridge, MA.
31 Product Information. Priftin (rifapentine). Hoechst Marion-Roussel Inc, Kansas City, MO.
32 Product Information. Intelence (etravirine). Ortho Biotech Inc, Bridgewater, NJ.
33 Product Information. Prezista (darunavir). Ortho Biotech Inc, Bridgewater, NJ.
34 Product Information. Orladeyo (berotralstat). BioCryst Pharmaceuticals Inc, Durham, NC.
35 Product Information. Alunbrig (brigatinib). Ariad Pharmaceuticals Inc, Cambridge, MA.
36 Product Information. Lorbrena (lorlatinib). Pfizer U.S. Pharmaceuticals Group, New York, NY.
37 Product Information. Zydelig (idelalisib). Gilead Sciences, Foster City, CA.
38 Product Information. Copiktra (duvelisib). Verastem, Inc., Needham, MA.
39 Product Information. Exjade (deferasirox). Novartis Pharmaceuticals, East Hanover, NJ.
40 Product Information. Mestinon (pyridostigmine). ICN Pharmaceuticals Inc, Cost Mesa, CA.
41 Product Information. Tasigna (nilotinib). Novartis Pharmaceuticals, East Hanover, NJ.
42 Product Information. Sprycel (dasatinib). Bristol-Myers Squibb, Princeton, NJ.
43 Product Information. Motilium (domperidone). Janssen-Ortho Inc, Toronto, ON.
44 Beermann B, Groschinsky-Grind M "Enhancement of the gastrointestinal absorption of hydrochlorothiazide by propantheline." Eur J Clin Pharmacol 13 (1978): 385-7. [PMID: 668798]
45 EMA. European Medicines Agency. European Union "EMA - List of medicines under additional monitoring.".
46 Algeri S, Cerletti C, Curcio M, et al. "Effect of anticholinergic drugs on gastro-intestinal absorption of L-dopa in rats and man." Eur J Pharmacol 35 (1976): 293-9. [PMID: 1248506]
47 Product Information. Xeglyze (abametapir topical). Dr. Reddy's Laboratories Inc, Upper Saddle River, NJ.
48 Product Information. Xenleta (lefamulin). Nabriva Therapeutics US, Inc., King of Prussia, PA.
49 Product Information. Zokinvy (lonafarnib). Eiger BioPharmaceuticals, Palo Alto, CA.
50 Benoist G, van Oort I, et al "Drug-drug interaction potential in men treated with enzalutamide: Mind the gap." Br J Clin Pharmacol 0 (2017): epub. [PMID: 28881501]
51 Product Information. Oxbryta (voxelotor). Global Blood Therapeutics, Inc., South San Francisco, CA.
52 Cerner Multum, Inc. "Australian Product Information.".
53 Doherty MM, Charman WN "The mucosa of the small intestine: how clinically relevant as an organ of drug metabolism?" Clin Pharmacokinet 41 (2002): 235-53. [PMID: 11978143]
54 DSouza DL, Levasseur LM, Nezamis J, Robbins DK, Simms L, Koch KM "Effect of alosetron on the pharmacokinetics of alprazolam." J Clin Pharmacol 41 (2001): 452-4. [PMID: 11304902]
55 Product Information. Tavalisse (fostamatinib). Rigel Pharmaceuticals, South San Francisco, CA.
56 Product Information. Symlin (pramlintide). Amphastar Pharmaceuticals Inc, South El Monte, CA.