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Cefpodoxime Proxetil - 65862-140-01 - (Cefpodoxime Proxetil)

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Drug Information of Cefpodoxime Proxetil

Product NDC: 65862-140
Proprietary Name: Cefpodoxime Proxetil
Non Proprietary Name: Cefpodoxime Proxetil
Active Ingredient(s): 50    mg/5mL & nbsp;   Cefpodoxime Proxetil
Administration Route(s): ORAL
Dosage Form(s): GRANULE, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefpodoxime Proxetil

Product NDC: 65862-140
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065409
Marketing Category: ANDA
Start Marketing Date: 20070608

Package Information of Cefpodoxime Proxetil

Package NDC: 65862-140-01
Package Description: 1 BOTTLE in 1 CARTON (65862-140-01) > 100 mL in 1 BOTTLE

NDC Information of Cefpodoxime Proxetil

NDC Code 65862-140-01
Proprietary Name Cefpodoxime Proxetil
Package Description 1 BOTTLE in 1 CARTON (65862-140-01) > 100 mL in 1 BOTTLE
Product NDC 65862-140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefpodoxime Proxetil
Dosage Form Name GRANULE, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070608
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFPODOXIME PROXETIL
Strength Number 50
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefpodoxime Proxetil


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