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heartburn releif - 0904-5529-87 - (Famotidine)

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Drug Information of heartburn releif

Product NDC: 0904-5529
Proprietary Name: heartburn releif
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 heartburn releif

Product NDC: 0904-5529
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075400
Marketing Category: ANDA
Start Marketing Date: 20090909

Package Information of heartburn releif

Package NDC: 0904-5529-87
Package Description: 3 BLISTER PACK in 1 CARTON (0904-5529-87) > 10 TABLET in 1 BLISTER PACK

NDC Information of heartburn releif

NDC Code 0904-5529-87
Proprietary Name heartburn releif
Package Description 3 BLISTER PACK in 1 CARTON (0904-5529-87) > 10 TABLET in 1 BLISTER PACK
Product NDC 0904-5529
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090909
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of heartburn releif


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