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Cefpodoxime proxetil
Banan, Vantin (cefpodoxime proxetil) is a small molecule pharmaceutical. Cefpodoxime proxetil was first approved as Vantin on 1992-08-07. It is used to treat bacterial pneumonia, bacterial skin diseases, bronchitis, community-acquired infections, and cystitis amongst others in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
stomatognathic diseasesD009057
respiratory tract diseasesD012140
otorhinolaryngologic diseasesD010038
urogenital diseasesD000091642
skin and connective tissue diseasesD017437
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Cefpodoxime proxetil
Tradename
Company
Number
Date
Products
VANTINPharmacia & UpjohnN-050674 DISCN1992-08-07
2 products, RLD
VANTINPharmacia & UpjohnN-050675 DISCN1992-08-07
2 products, RLD
BANANSankyoN-050687 DISCN1992-08-07
2 products
BANANSankyoN-050688 DISCN1992-08-07
2 products
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Labels
FDA
EMA
Brand Name
Status
Last Update
cefpodoxime proxetilANDA2023-06-19
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
bacterial pneumoniaEFO_1001272D018410J15.9
bacterial skin diseasesD017192
bronchitisD001991J40
community-acquired infectionsD017714
cystitisEFO_1000025D003556N30
escherichia coli infectionsEFO_1001318D004927B96.20
gonorrheaDOID_7551D006069A54
haemophilus infectionsEFO_1001127D006192
klebsiella infectionsEFO_1001353D007710
maxillary sinusitisEFO_0007361D015523J32.0
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Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
J01: Antibacterials for systemic use
J01D: Other beta-lactam antibacterials in atc
J01DD: Third-generation cephalosporins
J01DD13: Cefpodoxime
J01DD64: Cefpodoxime and beta-lactamase inhibitor
HCPCS
No data
Clinical
Clinical Trials
24 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Typhoid feverD014435EFO_0006789A01.022
Urinary tract infectionsD014552EFO_0003103N39.0112
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
SyphilisD013587EFO_0007504A53.91213
Uterine cervicitisD002575HP_0030160N7211
Bacterial vaginosisD016585EFO_000393211
Liver abscessD008100HP_0100523K75.011
Chronic renal insufficiencyD051436N1811
Vesico-ureteral refluxD014718EFO_0007536N13.711
HivD006678O98.711
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
GonorrheaD006069DOID_7551A54224
Chlamydia infectionsD002690EFO_0007205A74.911
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C8044
Bacterial infectionsD001424A49112
NeuroblastomaD009447EFO_000062111
DiarrheaD003967HP_0002014R19.711
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Postoperative complicationsD01118311
Laboratory infectionD00775711
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCEFPODOXIME PROXETIL
INNcefpodoxime
Description
Cefpodoxime is a third-generation cephalosporin antibiotic with methoxymethyl and (2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamino substituents at positions 3 and 7, respectively, of the cephem skeleton. Given by mouth as its proxetil ester prodrug, it is used to treat acute otitis media, pharyngitis, and sinusitis. It has a role as an antibacterial drug. It is a cephalosporin and a carboxylic acid.
Classification
Small molecule
Drug classcephalosporins
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
COCC1=C(C(=O)OC(C)OC(=O)OC(C)C)N2C(=O)[C@@H](NC(=O)/C(=N\OC)c3csc(N)n3)[C@H]2SC1
Identifiers
PDB
CAS-ID80210-62-4
RxCUI20489
ChEMBL IDCHEMBL1201016
ChEBI ID3505
PubChem CID6335986
DrugBankDB01416
UNII ID7R4F94TVGY (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 3,706 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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1,057 adverse events reported
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