General Information of Drug (ID: DMCFE9I)

Drug Name
Valproate
Synonyms
99-66-1; Dipropylacetic acid; Depakine; Depakene; 2-Propylvaleric acid; Ergenyl; Di-n-propylacetic acid; Mylproin; Pentanoic acid, 2-propyl-; 4-Heptanecarboxylic acid; Propylvaleric acid; n-Dipropylacetic acid; Myproic Acid; Di-n-propylessigsaure; n-DPA; Dipropylacetate; Convulex; Depakin; Vupral; Acido valproico; Acide valproique; Acidum valproicum; Stavzor; Avugane; Baceca; Kyselina 2-propylvalerova; 2-n-Propyl-n-valeric acid; Acetic acid, dipropyl-; Abbott 44090; Valproinsaeure; Savicol; Convulsofin; Deproic; VPA; Depakin chrono; Dipropyl Acetate; Med Valproic; Valproic acid USP; Valproic acid USP24; Acide valproique [INN-French]; Acido valproico [INN-Spanish]; Acidum valproicum [INN-Latin]; Alti-Valproic; Depakote (TM); Dom-Valproic; G2M-777; Kyselina 2-propylvalerova [Czech]; N-DPA; N-Dipropylacetic acid; Novo-Valproic; Nu-Valproic; PMS-Valproic Acid; Penta-Valproic; Valproic acid (USP); Di-n-propylessigsaeure; Di-n-propylessigsaure [German]; Valproic acid [USAN:INN:BAN]; Valproic Acid, SodiumSalt (2:1); 2 PP (base)
Indication
Disease Entry ICD 11 Status REF
Epilepsy 8A60-8A68 Approved [1]
Alcohol dependence 6C40.2 Phase 2 [2]
Therapeutic Class
Neurology Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 144.21
Logarithm of the Partition Coefficient (xlogp) 2.8
Rotatable Bond Count (rotbonds) 5
Hydrogen Bond Donor Count (hbonddonor) 1
Hydrogen Bond Acceptor Count (hbondacc) 2
ADMET Property
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [3]
Bioavailability
99% of drug becomes completely available to its intended biological destination(s) [4]
Clearance
The drug present in the plasma can be removed from the body at the rate of 0.16 mL/min/kg [5]
Elimination
1.8% of drug is excreted from urine in the unchanged form [3]
Half-life
The concentration or amount of drug in body reduced by one-half in 12 hours [5]
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 289.15057 micromolar/kg/day [6]
Unbound Fraction
The unbound fraction of drug in plasma is 0.08% [5]
Vd
Fluid volume that would be required to contain the amount of drug present in the body at the same concentration as in the plasma 0.14 L/kg [5]
Water Solubility
The ability of drug to dissolve in water is measured as 1.3 mg/mL [3]
Chemical Identifiers
Formula
C8H16O2
IUPAC Name
2-propylpentanoic acid
Canonical SMILES
CCCC(CCC)C(=O)O
InChI
InChI=1S/C8H16O2/c1-3-5-7(6-4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10)
InChIKey
NIJJYAXOARWZEE-UHFFFAOYSA-N
Cross-matching ID
PubChem CID
3121
ChEBI ID
CHEBI:39867
CAS Number
99-66-1
DrugBank ID
DB00313
TTD ID
D0Y3KG
VARIDT ID
DR00399
INTEDE ID
DR1667
ACDINA ID
D00717
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
Glycogen synthase kinase-3 alpha (GSK-3A) TTRZQE3 GSK3A_HUMAN Inhibitor [2]
Histone deacetylase (HDAC) TTBH0VX NOUNIPROTAC Inhibitor [7]

Drug Transporter (DTP)
DTP Name DTP ID UniProt ID MOA REF
Monocarboxylate transporter 2 (SLC16A7) DTLT3UG MOT2_HUMAN Substrate [8]
Multidrug resistance-associated protein 2 (ABCC2) DTFI42L MRP2_HUMAN Substrate [9]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 2C9 (CYP2C9) DE5IED8 CP2C9_HUMAN Substrate [10]
UDP-glucuronosyltransferase 1A1 (UGT1A1) DEYGVN4 UD11_HUMAN Substrate [11]
Mephenytoin 4-hydroxylase (CYP2C19) DEGTFWK CP2CJ_HUMAN Substrate [10]
Cytochrome P450 2A6 (CYP2A6) DEJVYAZ CP2A6_HUMAN Substrate [12]
Cytochrome P450 3A5 (CYP3A5) DEIBDNY CP3A5_HUMAN Substrate [13]
Cytochrome P450 2B6 (CYP2B6) DEPKLMQ CP2B6_HUMAN Substrate [14]
UDP-glucuronosyltransferase 2B7 (UGT2B7) DEB3CV1 UD2B7_HUMAN Substrate [15]
Prostaglandin G/H synthase 1 (COX-1) DE073H6 PGH1_HUMAN Substrate [13]
UDP-glucuronosyltransferase 1A9 (UGT1A9) DE85D2P UD19_HUMAN Substrate [13]
UDP-glucuronosyltransferase 1A10 (UGT1A10) DEL5N6Y UD110_HUMAN Substrate [16]
UDP-glucuronosyltransferase 1A6 (UGT1A6) DESD26P UD16_HUMAN Substrate [16]
UDP-glucuronosyltransferase 1A3 (UGT1A3) DEF2WXN UD13_HUMAN Substrate [11]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
(3R)-3-hydroxyacyl-CoA dehydrogenase (HSD17B8) OTX1DWEF DHB8_HUMAN Gene/Protein Processing [17]
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial (CYP24A1) OTG2T749 CP24A_HUMAN Gene/Protein Processing [18]
1,4-alpha-glucan-branching enzyme (GBE1) OTK2N05B GLGB_HUMAN Gene/Protein Processing [19]
1,5-anhydro-D-fructose reductase (AKR1E2) OT7GBQEB AKCL2_HUMAN Post-Translational Modifications [20]
1-acyl-sn-glycerol-3-phosphate acyltransferase beta (AGPAT2) OT5I4Y9K PLCB_HUMAN Gene/Protein Processing [21]
1-acyl-sn-glycerol-3-phosphate acyltransferase delta (AGPAT4) OT5CTQKO PLCD_HUMAN Gene/Protein Processing [19]
1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon (AGPAT5) OTNY3VMD PLCE_HUMAN Post-Translational Modifications [20]
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma (AGPAT3) OTAUR5TG PLCC_HUMAN Post-Translational Modifications [20]
1-acylglycerol-3-phosphate O-acyltransferase ABHD5 (ABHD5) OTY829Z3 ABHD5_HUMAN Gene/Protein Processing [22]
1-acylglycerol-3-phosphate O-acyltransferase PNPLA3 (PNPLA3) OTR4990X PLPL3_HUMAN Post-Translational Modifications [20]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Drug-Drug Interaction (DDI) Information of This Drug

Coadministration of a Drug Treating the Same Disease as Valproate
DDI Drug Name DDI Drug ID Severity Mechanism Disease REF
Primidone DM0WX6I Moderate Decreased metabolism of Valproate caused by Primidone mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [23]
Mephenytoin DM5UGDK Moderate Increased plasma concentration of Valproate and Mephenytoin due to competitive binding of plasma proteins. Epilepsy/seizure [8A61-8A6Z] [24]
Tiagabine DMKSQG0 Minor Increased plasma concentration of Valproate and Tiagabine due to competitive binding of plasma proteins. Epilepsy/seizure [8A61-8A6Z] [25]
Fosphenytoin DMOX3LB Moderate Increased plasma concentration of Valproate and Fosphenytoin due to competitive binding of plasma proteins. Epilepsy/seizure [8A61-8A6Z] [23]
Ethotoin DMXWOCP Moderate Increased plasma concentration of Valproate and Ethotoin due to competitive binding of plasma proteins. Epilepsy/seizure [8A61-8A6Z] [24]
Coadministration of a Drug Treating the Disease Different from Valproate (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Remdesivir DMBFZ6L Moderate Increased risk of hepatotoxicity by the combination of Valproate and Remdesivir. 1D6YCoronavirus Disease 2019 [1D6YCoronavirus Disease 2019] [26]
Arn-509 DMT81LZ Moderate Increased metabolism of Valproate caused by Arn-509 mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [27]
Nifedipine DMSVOZT Moderate Decreased metabolism of Valproate caused by Nifedipine mediated interference with first-pass metabolism. Angina pectoris [BA40] [28]
Bedaquiline DM3906J Moderate Increased risk of hepatotoxicity by the combination of Valproate and Bedaquiline. Antimicrobial drug resistance [MG50-MG52] [29]
Montelukast DMD157S Moderate Decreased metabolism of Valproate caused by Montelukast mediated inhibition of CYP450 enzyme. Asthma [CA23] [30]
Desipramine DMT2FDC Moderate Antagonize the effect of Valproate when combined with Desipramine. Attention deficit hyperactivity disorder [6A05] [31]
Lamotrigine DM8SXYG Major Decreased metabolism of Valproate caused by Lamotrigine mediated inhibition of UGT. Bipolar disorder [6A60] [32]
Pexidartinib DMS2J0Z Major Increased risk of hepatotoxicity by the combination of Valproate and Pexidartinib. Bone/articular cartilage neoplasm [2F7B] [33]
Nitazoxanide DMOWLVG Moderate Increased plasma concentration of Valproate and Nitazoxanide due to competitive binding of plasma proteins. Bowel habit change [ME05] [34]
Levomilnacipran DMV26S8 Moderate Antagonize the effect of Valproate when combined with Levomilnacipran. Chronic pain [MG30] [35]
Anisindione DM2C48U Moderate Increased plasma concentration of Valproate and Anisindione due to competitive binding of plasma proteins. Coagulation defect [3B10] [36]
Regorafenib DMHSY1I Moderate Decreased metabolism of Valproate caused by Regorafenib mediated inhibition of UGT. Colorectal cancer [2B91] [37]
Olopatadine DMKMWQG Moderate Additive CNS depression effects by the combination of Valproate and Olopatadine. Conjunctiva disorder [9A60] [38]
Nimodipine DMQ0RKZ Minor Decreased metabolism of Valproate caused by Nimodipine mediated interference with first-pass metabolism. Coronary vasospastic disease [BA85] [39]
Ethanol DMDRQZU Moderate Additive CNS depression effects by the combination of Valproate and Ethanol. Cystitis [GC00] [38]
Sertraline DM0FB1J Moderate Antagonize the effect of Valproate when combined with Sertraline. Depression [6A70-6A7Z] [35]
Trimipramine DM1SC8M Moderate Additive CNS depression effects by the combination of Valproate and Trimipramine. Depression [6A70-6A7Z] [31]
Imipramine DM2NUH3 Moderate Additive CNS depression effects by the combination of Valproate and Imipramine. Depression [6A70-6A7Z] [31]
Fluoxetine DM3PD2C Minor Decreased metabolism of Valproate caused by Fluoxetine. Depression [6A70-6A7Z] [40]
Nortriptyline DM4KDYJ Moderate Additive CNS depression effects by the combination of Valproate and Nortriptyline. Depression [6A70-6A7Z] [31]
Vilazodone DM4LECQ Moderate Antagonize the effect of Valproate when combined with Vilazodone. Depression [6A70-6A7Z] [35]
Paroxetine DM5PVQE Moderate Increased risk of hyponatremia by the combination of Valproate and Paroxetine. Depression [6A70-6A7Z] [35]
Vortioxetine DM6F1PU Moderate Increased risk of hyponatremia by the combination of Valproate and Vortioxetine. Depression [6A70-6A7Z] [35]
Duloxetine DM9BI7M Moderate Increased risk of hyponatremia by the combination of Valproate and Duloxetine. Depression [6A70-6A7Z] [35]
Milnacipran DMBFE74 Moderate Antagonize the effect of Valproate when combined with Milnacipran. Depression [6A70-6A7Z] [35]
Escitalopram DMFK9HG Moderate Increased risk of hyponatremia by the combination of Valproate and Escitalopram. Depression [6A70-6A7Z] [35]
Desvenlafaxine DMHD4PE Moderate Increased risk of hyponatremia by the combination of Valproate and Desvenlafaxine. Depression [6A70-6A7Z] [35]
Amitriptyline DMK7F9S Moderate Additive CNS depression effects by the combination of Valproate and Amitriptyline. Depression [6A70-6A7Z] [31]
Amoxapine DMKITQE Moderate Antagonize the effect of Valproate when combined with Amoxapine. Depression [6A70-6A7Z] [31]
Protriptyline DMNHTZI Moderate Antagonize the effect of Valproate when combined with Protriptyline. Depression [6A70-6A7Z] [31]
Doxepin DMPI98T Moderate Additive CNS depression effects by the combination of Valproate and Doxepin. Depression [6A70-6A7Z] [31]
Esketamine DMVU687 Moderate Additive CNS depression effects by the combination of Valproate and Esketamine. Depression [6A70-6A7Z] [26]
Cannabidiol DM0659E Moderate Increased risk of hepatotoxicity by the combination of Valproate and Cannabidiol. Epileptic encephalopathy [8A62] [27]
Brimonidine DMQLT4N Moderate Additive CNS depression effects by the combination of Valproate and Brimonidine. Glaucoma [9C61] [41]
Brentuximab vedotin DMWLC57 Moderate Increased risk of hepatotoxicity by the combination of Valproate and Brentuximab vedotin. Hodgkin lymphoma [2B30] [42]
Zidovudine DM4KI7O Moderate Decreased metabolism of Valproate caused by Zidovudine mediated inhibition of UGT. Human immunodeficiency virus disease [1C60-1C62] [43]
Efavirenz DMC0GSJ Moderate Increased risk of hepatotoxicity by the combination of Valproate and Efavirenz. Human immunodeficiency virus disease [1C60-1C62] [44]
Etravirine DMGV8QU Moderate Decreased metabolism of Valproate caused by Etravirine mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [45]
Ritonavir DMU764S Moderate Increased metabolism of Valproate caused by Ritonavir mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [26]
Fenofibrate DMFKXDY Moderate Decreased metabolism of Valproate caused by Fenofibrate mediated inhibition of CYP450 enzyme. Hyper-lipoproteinaemia [5C80] [26]
Mipomersen DMGSRN1 Major Increased risk of hepatotoxicity by the combination of Valproate and Mipomersen. Hyper-lipoproteinaemia [5C80] [46]
Teriflunomide DMQ2FKJ Major Increased risk of hepatotoxicity by the combination of Valproate and Teriflunomide. Hyper-lipoproteinaemia [5C80] [28]
BMS-201038 DMQTAGO Major Increased risk of hepatotoxicity by the combination of Valproate and BMS-201038. Hyper-lipoproteinaemia [5C80] [47]
Lesinurad DMUR64T Moderate Decreased metabolism of Valproate caused by Lesinurad mediated inhibition of CYP450 enzyme. Inborn purine/pyrimidine/nucleotide metabolism error [5C55] [48]
Methotrexate DM2TEOL Moderate Increased risk of hepatotoxicity by the combination of Valproate and Methotrexate. Leukaemia [2A60-2B33] [27]
Ceritinib DMB920Z Moderate Decreased metabolism of Valproate caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [26]
PF-06463922 DMKM7EW Moderate Increased metabolism of Valproate caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [26]
Chloroquine DMSI5CB Moderate Antagonize the effect of Valproate when combined with Chloroquine. Malaria [1F40-1F45] [26]
Hydroxychloroquine DMSIVND Moderate Antagonize the effect of Valproate when combined with Hydroxychloroquine. Malaria [1F40-1F45] [26]
Calaspargase pegol DMQZBXI Moderate Increased risk of hepatotoxicity by the combination of Valproate and Calaspargase pegol. Malignant haematopoietic neoplasm [2B33] [49]
Idelalisib DM602WT Moderate Increased risk of hepatotoxicity by the combination of Valproate and Idelalisib. Mature B-cell leukaemia [2A82] [50]
Clofarabine DMCVJ86 Moderate Increased risk of hepatotoxicity by the combination of Valproate and Clofarabine. Mature B-cell lymphoma [2A85] [51]
Arry-162 DM1P6FR Moderate Decreased clearance of Valproate due to the transporter inhibition by Arry-162. Melanoma [2C30] [26]
Lasmiditan DMXLVDT Moderate Additive CNS depression effects by the combination of Valproate and Lasmiditan. Migraine [8A80] [52]
Lanthanum carbonate DMMJQSH Moderate Decreased absorption of Valproate due to formation of complexes caused by Lanthanum carbonate. Mineral absorption/transport disorder [5C64] [28]
Flibanserin DM70DTN Moderate Additive CNS depression effects by the combination of Valproate and Flibanserin. Mood disorder [6A60-6E23] [53]
Thalidomide DM70BU5 Moderate Additive CNS depression effects by the combination of Valproate and Thalidomide. Multiple myeloma [2A83] [54]
Orlistat DMRJSP8 Moderate Altered absorption of Valproate caused by Orlistat. Obesity [5B80-5B81] [55]
Rucaparib DM9PVX8 Moderate Decreased metabolism of Valproate caused by Rucaparib mediated inhibition of UGT. Ovarian cancer [2C73] [56]
Dextropropoxyphene DM23HCX Major Additive CNS depression effects by the combination of Valproate and Dextropropoxyphene. Pain [MG30-MG3Z] [57]
Diflunisal DM7EN8I Moderate Increased plasma concentration of Valproate and Diflunisal due to competitive binding of plasma proteins. Pain [MG30-MG3Z] [58]
Ibuprofen DM8VCBE Minor Increased plasma concentration of Valproate and Ibuprofen due to competitive binding of plasma proteins. Pain [MG30-MG3Z] [59]
Buprenorphine DMPRI8G Major Additive CNS depression effects by the combination of Valproate and Buprenorphine. Pain [MG30-MG3Z] [60]
Meperidine DMX4GND Moderate Additive CNS depression effects by the combination of Valproate and Meperidine. Pain [MG30-MG3Z] [61]
Esomeprazole DM7BN0X Minor Increased plasma concentrations of Valproate and Esomeprazole due to competitive inhibition of the same metabolic pathway. Peptic ulcer [DA61] [62]
Choline salicylate DM8P137 Moderate Increased plasma concentration of Valproate and Choline salicylate due to competitive binding of plasma proteins. Postoperative inflammation [1A00-CA43] [58]
Lonafarnib DMGM2Z6 Moderate Decreased metabolism of Valproate caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [63]
Selexipag DMAHSU0 Moderate Decreased metabolism of Valproate caused by Selexipag mediated inhibition of UGT. Pulmonary hypertension [BB01] [26]
Salsalate DM13P4C Moderate Increased plasma concentration of Valproate and Salsalate due to competitive binding of plasma proteins. Rheumatoid arthritis [FA20] [58]
Celecoxib DM6LOQU Moderate Decreased metabolism of Valproate caused by Celecoxib mediated inhibition of CYP450 enzyme. Rheumatoid arthritis [FA20] [64]
Leflunomide DMR8ONJ Major Increased risk of hepatotoxicity by the combination of Valproate and Leflunomide. Rheumatoid arthritis [FA20] [28]
Paliperidone DM7NPJS Moderate Additive CNS depression effects by the combination of Valproate and Paliperidone. Schizophrenia [6A20] [27]
Risperidone DMN6DXL Moderate Increased plasma concentration of Valproate and Risperidone due to competitive binding of plasma proteins. Schizophrenia [6A20] [65]
Salicyclic acid DM2F8XZ Moderate Increased plasma concentration of Valproate and Salicyclic acid due to competitive binding of plasma proteins. Seborrhoeic dermatitis [EA81] [66]
Vardenafil DMTBGW8 Moderate Decreased metabolism of Valproate caused by Vardenafil mediated inhibition of CYP450 enzyme. Sexual dysfunction [HA00-HA01] [67]
Trabectedin DMG3Y89 Moderate Increased risk of hepatotoxicity by the combination of Valproate and Trabectedin. Solid tumour/cancer [2A00-2F9Z] [27]
Epirubicin DMPDW6T Moderate Increased risk of hepatotoxicity by the combination of Valproate and Epirubicin. Solid tumour/cancer [2A00-2F9Z] [26]
Pitolisant DM8RFNJ Moderate Accelerated clearance of Valproate due to the transporter induction by Pitolisant. Somnolence [MG42] [27]
Naltrexone DMUL45H Moderate Increased risk of hepatotoxicity by the combination of Valproate and Naltrexone. Substance abuse [6C40] [68]
Warfarin DMJYCVW Moderate Increased plasma concentration of Valproate and Warfarin due to competitive binding of plasma proteins. Supraventricular tachyarrhythmia [BC81] [36]
Lusutrombopag DMH6IKO Moderate Decreased clearance of Valproate due to the transporter inhibition by Lusutrombopag. Thrombocytopenia [3B64] [56]
Cetirizine DMOMP9U Moderate Additive CNS depression effects by the combination of Valproate and Cetirizine. Vasomotor/allergic rhinitis [CA08] [69]
⏷ Show the Full List of 82 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
Allura red AC dye E00338 33258 Colorant
D&C red no. 27 E00381 83511 Colorant
D&C red no. 28 E00491 6097185 Colorant
D&C red no. 30 E00456 3000709 Colorant
Diethyl phthalate E00135 6781 Plasticizing agent; Solvent
Ethyl acrylate E00191 8821 Film/membrane-forming agent; Flavoring agent
FD&C blue no. 1 E00263 19700 Colorant
FD&C blue no. 2 E00446 2723854 Colorant
Hydrazine yellow E00409 164825 Colorant
Isopropyl alcohol E00070 3776 Antimicrobial preservative; Solvent
Mannitol E00103 6251 Diluent; Flavoring agent; Lyophilization aid; Plasticizing agent; Tonicity agent
methylparaben E00149 7456 Antimicrobial preservative
Oleic acid E00421 445639 Emulsifying agent; Penetration agent; Solubilizing agent
Phenoxyisopropanol E00386 92839 Antimicrobial preservative
Propyl 4-hydroxybenzoate E00141 7175 Antimicrobial preservative
Quinoline yellow WS E00309 24671 Colorant
Sodium lauryl sulfate E00464 3423265 Emulsifying agent; Modified-release agent; Penetration agent; Solubilizing agent; Surfactant; lubricant
Stearic acid E00079 5281 Emulsifying agent; Solubilizing agent; Viscosity-controlling agent; lubricant
Sunset yellow FCF E00255 17730 Colorant
Vanillin E00049 1183 Flavoring agent
Acetone E00004 180 Solvent
Ammonia E00007 222 Alkalizing agent
Beta-D-lactose E00099 6134 Diluent; Dry powder inhaler carrier; Lyophilization aid
Brushite E00392 104805 Diluent
Butyl alcohol E00011 263 Flavoring agent; Solvent
Carmellose sodium E00625 Not Available Disintegrant
Crospovidone E00626 Not Available Disintegrant
Dextrin E00359 62698 Binding agent; Diluent; Microencapsulating agent; Stiffening agent; Suspending agent; Viscosity-controlling agent
Dibutyl sebacate E00160 7986 Plasticizing 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
Glyceryl behenate E00481 5362585 Binding agent; Coating agent; Flavoring agent; Modified-release agent; Viscosity-controlling agent; lubricant
Glyceryl dibehenate E00537 22477175 Binding agent; Coating agent; Flavoring agent; Modified-release agent; Viscosity-controlling agent; lubricant
Hypromellose E00634 Not Available Coating agent
Isobutyl alcohol E00130 6560 Flavoring agent; Solvent
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
Polyvinyl alcohol E00666 Not Available Coating agent; Emulsion stabilizing agent; Film/Membrane-forming agent
Potassium hydroxide E00233 14797 Alkalizing agent
Potassium sorbate E00566 23676745 Antimicrobial preservative
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 hydroxide E00234 14798 Alkalizing agent
Soybean lecithin E00637 Not Available Other agent
Talc E00520 16211421 Anticaking agent; Diluent; Glidant; lubricant
Titanium dioxide E00322 26042 Coating agent; Colorant; Opacifying agent
Triacetin E00080 5541 Humectant; Plasticizing agent; Solvent
Triethyl citrate E00128 6506 Plasticizing agent; Solvent
Vinylpyrrolidone E00668 Not Available Binding agent; Coating agent; Disintegrant; Film/membrane-forming agent; Solubilizing agent; Suspending agent
Water E00035 962 Solvent
⏷ Show the Full List of 59 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Valproic acid 250 mg tablet 250 mg Delayed Release Oral Tablet Oral
Valproic acid 500 mg tablet 500 mg Delayed Release Oral Tablet Oral
Valproic acid 125 mg tablet 125 mg Delayed Release Oral Tablet Oral
Valproic acid 125 mg capsule 125 mg Delayed Release Oral Capsule Oral
Valproic acid 125 mg tablet 125 mg Delayed Release Tablet Oral
Valproic acid 125 mg tablet 125 mg Enteric Coated Tablet Oral
Valproic acid 500 mg tablet 500 mg Enteric Coated Tablet Oral
Valproic acid 250 mg tablet 250 mg 24 HR Extended Release Tablet Oral
Valproic acid 500 mg tablet 500 mg 24 HR Extended Release Tablet Oral
Valproic acid 250 mg tablet 250 mg Enteric Coated Tablet Oral
Valproic acid 250 mg tablet 250 mg 24 HR Extended Release Oral Tablet Oral
Valproic acid 500 mg tablet 500 mg 24 HR Extended Release Oral Tablet Oral
Valproic acid 500 mg tablet 500 mg Delayed Release Tablet Oral
Valproic acid 250 mg capsule 250 mg Delayed Release Oral Capsule Oral
Valproic acid 500 mg capsule 500 mg Delayed Release Oral Capsule Oral
Valproic acid 250 mg capsule 250 mg Oral Capsule Oral
Valproic acid 250 mg tablet 250 mg Delayed Release Tablet Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

1 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7009).
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