Famotidine - 55648-936-03 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 55648-936
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 20    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 55648-936
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075786
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of Famotidine

Package NDC: 55648-936-03
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (55648-936-03)

NDC Information of Famotidine

NDC Code 55648-936-03
Proprietary Name Famotidine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (55648-936-03)
Product NDC 55648-936
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010416
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
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