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Metformin Hydrochloride - 49349-469-10 - (METFORMIN HYDROCHLORIDE)

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Drug Information of Metformin Hydrochloride

Product NDC: 49349-469
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: METFORMIN HYDROCHLORIDE
Active Ingredient(s): 1000    mg/1 & nbsp;   METFORMIN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 49349-469
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077064
Marketing Category: ANDA
Start Marketing Date: 20120827

Package Information of Metformin Hydrochloride

Package NDC: 49349-469-10
Package Description: 6 TABLET in 1 BLISTER PACK (49349-469-10)

NDC Information of Metformin Hydrochloride

NDC Code 49349-469-10
Proprietary Name Metformin Hydrochloride
Package Description 6 TABLET in 1 BLISTER PACK (49349-469-10)
Product NDC 49349-469
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120827
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


General Information