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Metformin hydrochloride - 63629-1396-1 - (Metformin hydrochloride)

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Drug Information of Metformin hydrochloride

Product NDC: 63629-1396
Proprietary Name: Metformin hydrochloride
Non Proprietary Name: Metformin hydrochloride
Active Ingredient(s): 850    mg/1 & nbsp;   Metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin hydrochloride

Product NDC: 63629-1396
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079148
Marketing Category: ANDA
Start Marketing Date: 20090603

Package Information of Metformin hydrochloride

Package NDC: 63629-1396-1
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (63629-1396-1)

NDC Information of Metformin hydrochloride

NDC Code 63629-1396-1
Proprietary Name Metformin hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (63629-1396-1)
Product NDC 63629-1396
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090603
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin hydrochloride


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