Famotidine - 35356-730-90 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 35356-730
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: 35356-730
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075786
Marketing Category: ANDA
Start Marketing Date: 20120727

Package Information of Famotidine

Package NDC: 35356-730-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (35356-730-90)

NDC Information of Famotidine

NDC Code 35356-730-90
Proprietary Name Famotidine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (35356-730-90)
Product NDC 35356-730
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 Lake Erie Medical DBA Quality Care Products LLC
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