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Health Mart Famotidine - 62011-0143-1 - (Famotidine)

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Drug Information of Health Mart Famotidine

Product NDC: 62011-0143
Proprietary Name: Health Mart 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 Health Mart Famotidine

Product NDC: 62011-0143
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077351
Marketing Category: ANDA
Start Marketing Date: 20120320

Package Information of Health Mart Famotidine

Package NDC: 62011-0143-1
Package Description: 5 BLISTER PACK in 1 CARTON (62011-0143-1) > 5 TABLET in 1 BLISTER PACK

NDC Information of Health Mart Famotidine

NDC Code 62011-0143-1
Proprietary Name Health Mart Famotidine
Package Description 5 BLISTER PACK in 1 CARTON (62011-0143-1) > 5 TABLET in 1 BLISTER PACK
Product NDC 62011-0143
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120320
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Health Mart Famotidine


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