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Cefpodoxime Proxetil - 0781-5438-20 - (Cefpodoxime Proxetil)

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Drug Information of Cefpodoxime Proxetil

Product NDC: 0781-5438
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: 0781-5438
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065462
Marketing Category: ANDA
Start Marketing Date: 20080528

Package Information of Cefpodoxime Proxetil

Package NDC: 0781-5438-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (0781-5438-20)

NDC Information of Cefpodoxime Proxetil

NDC Code 0781-5438-20
Proprietary Name Cefpodoxime Proxetil
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (0781-5438-20)
Product NDC 0781-5438
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefpodoxime Proxetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080528
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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