Famotidine - 52125-658-02 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 52125-658
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 20    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 52125-658
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075805
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Famotidine

Package NDC: 52125-658-02
Package Description: 30 TABLET in 1 VIAL (52125-658-02)

NDC Information of Famotidine

NDC Code 52125-658-02
Proprietary Name Famotidine
Package Description 30 TABLET in 1 VIAL (52125-658-02)
Product NDC 52125-658
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Famotidine


General Information