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CEFPODOXIME PROXETIL - 65862-095-99 - (CEFPODOXIME PROXETIL)

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Drug Information of CEFPODOXIME PROXETIL

Product NDC: 65862-095
Proprietary Name: CEFPODOXIME PROXETIL
Non Proprietary Name: CEFPODOXIME PROXETIL
Active Ingredient(s): 100    mg/1 & nbsp;   CEFPODOXIME PROXETIL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CEFPODOXIME PROXETIL

Product NDC: 65862-095
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065370
Marketing Category: ANDA
Start Marketing Date: 20070611

Package Information of CEFPODOXIME PROXETIL

Package NDC: 65862-095-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)

NDC Information of CEFPODOXIME PROXETIL

NDC Code 65862-095-99
Proprietary Name CEFPODOXIME PROXETIL
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)
Product NDC 65862-095
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFPODOXIME PROXETIL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070611
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFPODOXIME PROXETIL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFPODOXIME PROXETIL


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