Famotidine - 68788-9779-8 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 68788-9779
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 40    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: 68788-9779
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075786
Marketing Category: ANDA
Start Marketing Date: 20120727

Package Information of Famotidine

Package NDC: 68788-9779-8
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (68788-9779-8)

NDC Information of Famotidine

NDC Code 68788-9779-8
Proprietary Name Famotidine
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (68788-9779-8)
Product NDC 68788-9779
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120727
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name FAMOTIDINE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Famotidine


General Information