Famotidine - 61442-121-01 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 61442-121
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: 61442-121
Labeler Name: Carlsbad Technology, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075805
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of Famotidine

Package NDC: 61442-121-01
Package Description: 24 BOTTLE in 1 BOX (61442-121-01) > 100 TABLET in 1 BOTTLE

NDC Information of Famotidine

NDC Code 61442-121-01
Proprietary Name Famotidine
Package Description 24 BOTTLE in 1 BOX (61442-121-01) > 100 TABLET in 1 BOTTLE
Product NDC 61442-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010416
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, 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