Famotidine - 55289-765-30 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 55289-765
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: 55289-765
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075511
Marketing Category: ANDA
Start Marketing Date: 20110211

Package Information of Famotidine

Package NDC: 55289-765-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-765-30)

NDC Information of Famotidine

NDC Code 55289-765-30
Proprietary Name Famotidine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-765-30)
Product NDC 55289-765
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110211
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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