General Information of Drug (ID: DMSVOCZ)

Drug Name
Pantoprazole
Synonyms
Astropan; Pantoprazol; Pantoprazolum; Pantoprozole; Pantor; Pantozol; Protium; Protonix; Somac; Pantoprazole Na; Pantoprazole Sodium; Protonix IV; BY 1023; Astropan (TN); BY-1023; Controloc (TN); Inipomp (TN); Pantecta (TN); Pantoloc (TN); Pantopan (TN); Pantoprazol [INN-Spanish]; Pantoprazolum [INN-Latin]; Pantor (TN); Pantotab (TN); Pantozol (TN); Protium (TN); Protonix (TN); SK&F 96022; SK-96022; SKF-96022; Somac (TN); Ulcepraz (TN); Pantoprazole (USAN/INN); Pantoprazole [USAN:BAN:INN]; SK&F-96022; 5-(Difluoromethoxy)-2-(((3,4-dimethoxy-2-pyridyl)methyl)sulfinyl)benzimidazole; 5-(difluoromethoxy)-2-{[(3,4-dimethoxypyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole; 6-(difluoromethoxy)-2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]-1H-benzimidazole
Indication
Disease Entry ICD 11 Status REF
Gastrinoma 2C10.1 Approved [1]
Gastroesophageal reflux disease DA22.Z Approved [2]
Peptic ulcer DA61 Approved [1]
Therapeutic Class
Antiulcer Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 383.4
Logarithm of the Partition Coefficient (xlogp) 2.4
Rotatable Bond Count (rotbonds) 7
Hydrogen Bond Donor Count (hbonddonor) 1
Hydrogen Bond Acceptor Count (hbondacc) 9
ADMET Property
Absorption AUC
The area under the plot of plasma concentration (AUC) of drug is 5 mgh/L [3]
Absorption Cmax
The maximum plasma concentration (Cmax) of drug is 2.5 mg/L [3]
Absorption Tmax
The time to maximum plasma concentration (Tmax) is 2-3 h [3]
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [4]
Bioavailability
The bioavailability of drug is 77% [3]
Clearance
The total clearance of drug is 7.6-14.0 L/h []
Elimination
After a single oral or intravenous (IV) dose of 14C-labeled pantoprazole to healthy, normal metabolizing subjects, about 71% of the dose was excreted in the urine, with 18% excreted in the feces by biliary excretion []
Half-life
The concentration or amount of drug in body reduced by one-half in 1 hours []
Metabolism
The drug is metabolized via the liver []
MRTD
The Maximum Recommended Therapeutic Dose (MRTD) of drug that ensured maximising efficacy and moderate side effect is 1.7398 micromolar/kg/day [5]
Unbound Fraction
The unbound fraction of drug in plasma is 0.02% [6]
Vd
The volume of distribution (Vd) of drug is 11.0-23.6 L []
Chemical Identifiers
Formula
C16H15F2N3O4S
IUPAC Name
6-(difluoromethoxy)-2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]-1H-benzimidazole
Canonical SMILES
COC1=C(C(=NC=C1)CS(=O)C2=NC3=C(N2)C=C(C=C3)OC(F)F)OC
InChI
InChI=1S/C16H15F2N3O4S/c1-23-13-5-6-19-12(14(13)24-2)8-26(22)16-20-10-4-3-9(25-15(17)18)7-11(10)21-16/h3-7,15H,8H2,1-2H3,(H,20,21)
InChIKey
IQPSEEYGBUAQFF-UHFFFAOYSA-N
Cross-matching ID
PubChem CID
4679
ChEBI ID
CHEBI:7915
CAS Number
102625-70-7
DrugBank ID
DB00213
TTD ID
D0T6XX
VARIDT ID
DR00458
INTEDE ID
DR1236
ACDINA ID
D00508
Combinatorial Drugs (CBD) Click to Jump to the Detailed CBD Information of This Drug
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
Gastric H(+)/K(+) ATPase (Proton pump) TTLOKXP ATP4A_HUMAN ; ATP4B_HUMAN Modulator [7]

Drug Transporter (DTP)
DTP Name DTP ID UniProt ID MOA REF
Breast cancer resistance protein (ABCG2) DTI7UX6 ABCG2_HUMAN Substrate [8]
P-glycoprotein 1 (ABCB1) DTUGYRD MDR1_HUMAN Substrate [9]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 3A4 (CYP3A4)
Main DME
DE4LYSA CP3A4_HUMAN Substrate [10]
Mephenytoin 4-hydroxylase (CYP2C19)
Main DME
DEGTFWK CP2CJ_HUMAN Substrate [11]
Cytochrome P450 1A2 (CYP1A2) DEJGDUW CP1A2_HUMAN Substrate [12]
Sulfotransferase 1A1 (SULT1A1) DEYWLRK ST1A1_HUMAN Substrate [10]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Hepcidin (HAMP) OT607RBL HEPC_HUMAN Gene/Protein Processing [13]
Phospholipid-transporting ATPase ABCA1 (ABCA1) OT94G6BQ ABCA1_HUMAN Gene/Protein Processing [14]
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 Disease Different from Pantoprazole (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Cefuroxime DMSIMD8 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Cefuroxime. Acute bronchitis [CA42] [15]
Framycetin DMF8DNE Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Framycetin. Alcoholic liver disease [DB94] [16]
Paromomycin DM1AGXN Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Paromomycin. Amoebiasis [1A36] [16]
Voriconazole DMAOL2S Moderate Decreased metabolism of Pantoprazole caused by Voriconazole mediated inhibition of CYP450 enzyme. Aspergillosis [1F20] [17]
Posaconazole DMUL5EW Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Posaconazole. Aspergillosis [1F20] [18]
Kanamycin DM2DMPO Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Kanamycin. Bacterial infection [1A00-1C4Z] [16]
Amikacin DM5PDRB Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Amikacin. Bacterial infection [1A00-1C4Z] [16]
Streptomycin DME1LQN Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Streptomycin. Bacterial infection [1A00-1C4Z] [16]
Cefpodoxime DMJUNY5 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Cefpodoxime. Bacterial infection [1A00-1C4Z] [15]
Gentamicin DMKINJO Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Gentamicin. Bacterial infection [1A00-1C4Z] [16]
Capreomycin DMNZBRY Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Capreomycin. Bacterial infection [1A00-1C4Z] [16]
Bacampicillin DMP54C7 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Bacampicillin. Bacterial infection [1A00-1C4Z] [15]
Netilmicin DMRD1QK Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Netilmicin. Bacterial infection [1A00-1C4Z] [16]
Cefditoren DMSUVM1 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Cefditoren. Bacterial infection [1A00-1C4Z] [19]
Tobramycin DMUI0CH Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Tobramycin. Bacterial infection [1A00-1C4Z] [16]
Vismodegib DM5IXKQ Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Vismodegib. Basal cell carcinoma [2C32] [20]
Pexidartinib DMS2J0Z Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Pexidartinib. Bone/articular cartilage neoplasm [2F7B] [21]
HKI-272 DM6QOVN Major Decreased absorption of Pantoprazole due to altered gastric pH caused by HKI-272. Breast cancer [2C60-2C6Y] [20]
Alpelisib DMEXMYK Moderate Increased metabolism of Pantoprazole caused by Alpelisib mediated induction of CYP450 enzyme. Breast cancer [2C60-2C6Y] [22]
Bosutinib DMTI8YE Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Bosutinib. Breast cancer [2C60-2C6Y] [23]
Atorvastatin DMF28YC Moderate Increased plasma concentrations of Pantoprazole and Atorvastatin due to competitive inhibition of the same metabolic pathway. Cardiovascular disease [BA00-BE2Z] [24]
Anisindione DM2C48U Moderate Decreased metabolism of Pantoprazole caused by Anisindione mediated inhibition of CYP450 enzyme. Coagulation defect [3B10] [25]
Panitumumab DMQPD1F Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Panitumumab. Colorectal cancer [2B91] [16]
Osilodrostat DMIJC9X Moderate Decreased metabolism of Pantoprazole caused by Osilodrostat mediated inhibition of CYP450 enzyme. Cushing syndrome [5A70] [26]
Lumacaftor DMCLWDJ Moderate Increased metabolism of Pantoprazole caused by Lumacaftor mediated induction of CYP450 enzyme. Cystic fibrosis [CA25] [27]
MK-8228 DMOB58Q Moderate Increased metabolism of Pantoprazole caused by MK-8228 mediated induction of CYP450 enzyme. Cytomegaloviral disease [1D82] [28]
Duloxetine DM9BI7M Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Duloxetine. Depression [6A70-6A7Z] [29]
Oxcarbazepine DM5PU6O Moderate Decreased metabolism of Pantoprazole caused by Oxcarbazepine mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [20]
Cenobamate DM8KLU9 Moderate Decreased metabolism of Pantoprazole caused by Cenobamate mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [30]
Brivaracetam DMSEPK8 Minor Decreased metabolism of Pantoprazole caused by Brivaracetam mediated inhibition of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [31]
Ethacrynic acid DM60QMR Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Ethacrynic acid. Essential hypertension [BA00] [32]
Bendroflumethiazide DM7EVLC Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Bendroflumethiazide. Essential hypertension [BA00] [16]
Benzthiazide DMQWZ0H Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Benzthiazide. Essential hypertension [BA00] [16]
Itraconazole DMCR1MV Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Itraconazole. Fungal infection [1F29-1F2F] [33]
Pentamidine DMHZJCG Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Pentamidine. Fungal infection [1F29-1F2F] [16]
Ketoconazole DMPZI3Q Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Ketoconazole. Fungal infection [1F29-1F2F] [33]
Amphotericin B DMTAJQE Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Amphotericin B. Fungal infection [1F29-1F2F] [16]
Chlorothiazide DMLHESP Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Chlorothiazide. Heart failure [BD10-BD1Z] [16]
Furosemide DMMQ8ZG Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Furosemide. Heart failure [BD10-BD1Z] [16]
Digoxin DMQCTIH Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Digoxin. Heart failure [BD10-BD1Z] [34]
Bumetanide DMRV7H0 Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Bumetanide. Heart failure [BD10-BD1Z] [16]
Hydroflumethiazide DMVPUQI Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Hydroflumethiazide. Heart failure [BD10-BD1Z] [16]
Torasemide DMXKJ6C Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Torasemide. Heart failure [BD10-BD1Z] [32]
GS-5885 DMSL3DX Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by GS-5885. Hepatitis virus infection [1E50-1E51] [20]
Rifampin DMA8J1G Moderate Increased metabolism of Pantoprazole caused by Rifampin mediated induction of CYP450 enzyme. HIV-infected patients with tuberculosis [1B10-1B14] [31]
Indinavir DM0T3YH Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Indinavir. Human immunodeficiency virus disease [1C60-1C62] [35]
Delavirdine DM3NF5G Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Delavirdine. Human immunodeficiency virus disease [1C60-1C62] [36]
Fosamprenavir DM4W9B3 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Fosamprenavir. Human immunodeficiency virus disease [1C60-1C62] [37]
Etravirine DMGV8QU Moderate Decreased metabolism of Pantoprazole caused by Etravirine mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [38]
Rilpivirine DMJ0QOW Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Rilpivirine. Human immunodeficiency virus disease [1C60-1C62] [39]
Atazanavir DMSYRBX Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Atazanavir. Human immunodeficiency virus disease [1C60-1C62] [40]
Raltegravir DMYURI6 Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Raltegravir. Human immunodeficiency virus disease [1C60-1C62] [41]
Simvastatin DM30SGU Moderate Decreased clearance of Pantoprazole and Simvastatin due to competitive inhibition of the same transporter. Hyper-lipoproteinaemia [5C80] [24]
Lovastatin DM9OZWQ Moderate Increased plasma concentrations of Pantoprazole and Lovastatin due to competitive inhibition of the same metabolic pathway. Hyper-lipoproteinaemia [5C80] [24]
Fenofibrate DMFKXDY Moderate Decreased metabolism of Pantoprazole caused by Fenofibrate mediated inhibition of CYP450 enzyme. Hyper-lipoproteinaemia [5C80] [20]
Indapamide DMGN1PW Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Indapamide. Hypertension [BA00-BA04] [16]
Trichlormethiazide DMHAQCO Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Trichlormethiazide. Hypertension [BA00-BA04] [16]
Hydrochlorothiazide DMUSZHD Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Hydrochlorothiazide. Hypertension [BA00-BA04] [16]
Liothyronine DM6IR3P Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Liothyronine. Hypo-thyroidism [5A00] [20]
Levothyroxine DMHN027 Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Levothyroxine. Hypo-thyroidism [5A00] [20]
Iron DMAP8MV Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Iron. Iron deficiency anaemia [3A00] [42]
Glycerol phenylbutyrate DMDGRQO Moderate Decreased metabolism of Pantoprazole caused by Glycerol phenylbutyrate mediated inhibition of CYP450 enzyme. Liver disease [DB90-DB9Z] [31]
Porfimer Sodium DM7ZWNY Moderate Increased risk of photosensitivity reactions by the combination of Pantoprazole and Porfimer Sodium. Lung cancer [2C25] [43]
Ceritinib DMB920Z Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Ceritinib. Lung cancer [2C25] [44]
Erlotinib DMCMBHA Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Erlotinib. Lung cancer [2C25] [20]
PF-06463922 DMKM7EW Moderate Increased metabolism of Pantoprazole caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [20]
Dacomitinib DMOH8VY Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Dacomitinib. Lung cancer [2C25] [31]
Selpercatinib DMZR15V Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Selpercatinib. Lung cancer [2C25] [31]
IPI-145 DMWA24P Moderate Decreased metabolism of Pantoprazole caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [45]
Acalabrutinib DM7GCVW Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Acalabrutinib. Mature B-cell lymphoma [2A85] [46]
Ponatinib DMYGJQO Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Ponatinib. Mature B-cell lymphoma [2A85] [20]
Flibanserin DM70DTN Moderate Decreased metabolism of Pantoprazole caused by Flibanserin mediated inhibition of CYP450 enzyme. Mood disorder [6A60-6E23] [47]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Pantoprazole caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [31]
Nilotinib DM7HXWT Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Nilotinib. Myeloproliferative neoplasm [2A20] [48]
Dasatinib DMJV2EK Major Decreased absorption of Pantoprazole due to altered gastric pH caused by Dasatinib. Myeloproliferative neoplasm [2A20] [49]
Prasugrel DM7MT6E Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Prasugrel. Myocardial infarction [BA41-BA43] [50]
Modafinil DMYILBE Moderate Decreased metabolism of Pantoprazole caused by Modafinil mediated inhibition of CYP450 enzyme. Narcolepsy [7A20] [20]
Chlorthalidone DM4DMBT Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Chlorthalidone. Oedema [MG29] [16]
Metolazone DMB39LO Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Metolazone. Oedema [MG29] [16]
Polythiazide DMCH80F Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Polythiazide. Oedema [MG29] [16]
Naproxen DMZ5RGV Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Naproxen. Osteoarthritis [FA00-FA05] [51]
Carboplatin DMG281S Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Carboplatin. Ovarian cancer [2C73] [16]
Aspirin DM672AH Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Aspirin. Pain [MG30-MG3Z] [52]
Abametapir DM2RX0I Moderate Decreased metabolism of Pantoprazole caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [53]
Choline salicylate DM8P137 Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Choline salicylate. Postoperative inflammation [1A00-CA43] [52]
Lonafarnib DMGM2Z6 Moderate Decreased metabolism of Pantoprazole caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [54]
Enzalutamide DMGL19D Moderate Accelerated clearance of Pantoprazole due to the transporter induction by Enzalutamide. Prostate cancer [2C82] [55]
Riociguat DMXBLMP Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Riociguat. Pulmonary hypertension [BB01] [56]
Axitinib DMGVH6N Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Axitinib. Renal cell carcinoma [2C90] [57]
Salsalate DM13P4C Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Salsalate. Rheumatoid arthritis [FA20] [52]
Salicyclic acid DM2F8XZ Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Salicyclic acid. Seborrhoeic dermatitis [EA81] [52]
Gefitinib DM15F0X Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Gefitinib. Solid tumour/cancer [2A00-2F9Z] [58]
Larotrectinib DM26CQR Moderate Decreased metabolism of Pantoprazole caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [20]
Armodafinil DMGB035 Moderate Decreased metabolism of Pantoprazole caused by Armodafinil mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [20]
Cisplatin DMRHGI9 Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Cisplatin. Solid tumour/cancer [2A00-2F9Z] [16]
Vandetanib DMRICNP Minor Decreased absorption of Pantoprazole due to altered gastric pH caused by Vandetanib. Solid tumour/cancer [2A00-2F9Z] [20]
Warfarin DMJYCVW Moderate Decreased metabolism of Pantoprazole caused by Warfarin mediated inhibition of CYP450 enzyme. Supraventricular tachyarrhythmia [BC81] [25]
Fostamatinib DM6AUHV Moderate Decreased clearance of Pantoprazole due to the transporter inhibition by Fostamatinib. Thrombocytopenia [3B64] [59]
Dicumarol DMFQCB1 Moderate Decreased metabolism of Pantoprazole caused by Dicumarol mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [60]
Clopidogrel DMOL54H Moderate Decreased metabolism of Pantoprazole caused by Clopidogrel mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [61]
Mycophenolate mofetil DMPQAGE Moderate Decreased absorption of Pantoprazole due to altered gastric pH caused by Mycophenolate mofetil. Transplant rejection [NE84] [62]
Tacrolimus DMZ7XNQ Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Tacrolimus. Transplant rejection [NE84] [20]
Plazomicin DMKMBES Moderate Increased risk of hypomagnesemia by the combination of Pantoprazole and Plazomicin. Urinary tract infection [GC08] [16]
⏷ Show the Full List of 103 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
Calcium carbonate E00198 10112 Binding agent; Buffering agent; Diluent; Opacifying agent
FD&C blue no. 2 E00446 2723854 Colorant
Isopropyl alcohol E00070 3776 Antimicrobial preservative; Solvent
Mannitol E00103 6251 Diluent; Flavoring agent; Lyophilization aid; Plasticizing agent; Tonicity agent
Quinoline yellow WS E00309 24671 Colorant
Sodium lauryl sulfate E00464 3423265 Emulsifying agent; Modified-release agent; Penetration agent; Solubilizing agent; Surfactant; lubricant
Sodium stearyl fumarate E00545 23665634 lubricant
Stearic acid E00079 5281 Emulsifying agent; Solubilizing agent; Viscosity-controlling agent; lubricant
Sunset yellow FCF E00255 17730 Colorant
Ammonia E00007 222 Alkalizing agent
Beta-D-lactose E00099 6134 Diluent; Dry powder inhaler carrier; Lyophilization aid
Butyl alcohol E00011 263 Flavoring agent; Solvent
Calcium stearate E00244 15324 lubricant
Carbonic acid disodium salt E00199 10340 Alkalizing agent; Buffering agent; Diluent; Dispersing agent
Crospovidone E00626 Not Available Disintegrant
Eisenoxyd E00585 56841934 Colorant
Ferric hydroxide oxide yellow E00539 23320441 Colorant
Ferrosoferric oxide E00231 14789 Colorant
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
Hydroxypropyl cellulose E00632 Not Available Binding agent; Coating agent; Emulsifying agent; Film/Membrane-forming agent; Modified-release agent; Suspending agent; Viscosity-controlling agent
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
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
Polyethylene glycol 6000 E00655 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
Propylene glycol distearate E00395 110800 Emollient; Opacifying agent; Surfactant
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 carbonate decahydrate E00405 151402 Alkalizing agent; Buffering agent; Diluent; Dispersing agent
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
Triethyl citrate E00128 6506 Plasticizing agent; Solvent
⏷ Show the Full List of 39 Pharmaceutical Excipients of This Drug
Pharmaceutical Formulation
Formulation Name Drug Dosage Dosage Form Route
Pantoprazole 20 mg tablet 20 mg Delayed Release Oral Tablet Oral
Pantoprazole 40 mg tablet 40 mg Delayed Release Oral Tablet Oral
Jump to Detail Pharmaceutical Formulation Page of This Drug

References

1 Pantoprazole FDA Label
2 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: 7260).
3 Bardou M, Martin J: Pantoprazole: from drug metabolism to clinical relevance. Expert Opin Drug Metab Toxicol. 2008 Apr;4(4):471-83. doi: 10.1517/17425255.4.4.471 .
4 BDDCS applied to over 900 drugs
5 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
6 Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 1352 Drug Compounds
7 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
8 Mechanism of the pharmacokinetic interaction between methotrexate and benzimidazoles: potential role for breast cancer resistance protein in clinical drug-drug interactions. Cancer Res. 2004 Aug 15;64(16):5804-11.
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