Famotidine - 0172-5729-10 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 0172-5729
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: 0172-5729
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075511
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of Famotidine

Package NDC: 0172-5729-10
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-5729-10) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0172-5729-00)

NDC Information of Famotidine

NDC Code 0172-5729-10
Proprietary Name Famotidine
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-5729-10) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0172-5729-00)
Product NDC 0172-5729
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 IVAX 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