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Metformin Hydrochloride - 63629-4810-1 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 63629-4810
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: metformin hydrochloride
Active Ingredient(s): 750    mg/1 & nbsp;   metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 63629-4810
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076706
Marketing Category: ANDA
Start Marketing Date: 20051229

Package Information of Metformin Hydrochloride

Package NDC: 63629-4810-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4810-1)

NDC Information of Metformin Hydrochloride

NDC Code 63629-4810-1
Proprietary Name Metformin Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4810-1)
Product NDC 63629-4810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20051229
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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