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Metfomin Hydrochloride - 49349-470-24 - (Metformin Hydrochloride)

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Drug Information of Metfomin Hydrochloride

Product NDC: 49349-470
Proprietary Name: Metfomin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 850    mg/1 & nbsp;   Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metfomin Hydrochloride

Product NDC: 49349-470
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077095
Marketing Category: ANDA
Start Marketing Date: 20110810

Package Information of Metfomin Hydrochloride

Package NDC: 49349-470-24
Package Description: 200 TABLET in 1 CANISTER (49349-470-24)

NDC Information of Metfomin Hydrochloride

NDC Code 49349-470-24
Proprietary Name Metfomin Hydrochloride
Package Description 200 TABLET in 1 CANISTER (49349-470-24)
Product NDC 49349-470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110810
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metfomin Hydrochloride


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