Vantin - 55289-390-02 - (cefpodoxime proxetil)

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Drug Information of Vantin

Product NDC: 55289-390
Proprietary Name: Vantin
Non Proprietary Name: cefpodoxime proxetil
Active Ingredient(s): 200    mg/1 & nbsp;   cefpodoxime proxetil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Vantin

Product NDC: 55289-390
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050674
Marketing Category: NDA
Start Marketing Date: 19910829

Package Information of Vantin

Package NDC: 55289-390-02
Package Description: 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-390-02)

NDC Information of Vantin

NDC Code 55289-390-02
Proprietary Name Vantin
Package Description 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-390-02)
Product NDC 55289-390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefpodoxime proxetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19910829
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CEFPODOXIME PROXETIL
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Vantin


General Information