FAMOTIDINE - 0172-2662-46 - (Famotidine)

Alphabetical Index


Drug Information of FAMOTIDINE

Product NDC: 0172-2662
Proprietary Name: FAMOTIDINE
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FAMOTIDINE

Product NDC: 0172-2662
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075512
Marketing Category: ANDA
Start Marketing Date: 20100218

Package Information of FAMOTIDINE

Package NDC: 0172-2662-46
Package Description: 30 BLISTER PACK in 1 CARTON (0172-2662-46) > 1 TABLET in 1 BLISTER PACK (0172-2662-00)

NDC Information of FAMOTIDINE

NDC Code 0172-2662-46
Proprietary Name FAMOTIDINE
Package Description 30 BLISTER PACK in 1 CARTON (0172-2662-46) > 1 TABLET in 1 BLISTER PACK (0172-2662-00)
Product NDC 0172-2662
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100218
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals, Inc.
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FAMOTIDINE


General Information