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Metformin Hydrochloride Extended Release - 49349-201-02 - (Metformin Hydrochloride Extended Release)

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Drug Information of Metformin Hydrochloride Extended Release

Product NDC: 49349-201
Proprietary Name: Metformin Hydrochloride Extended Release
Non Proprietary Name: Metformin Hydrochloride Extended Release
Active Ingredient(s): 500    mg/1 & nbsp;   Metformin Hydrochloride Extended Release
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride Extended Release

Product NDC: 49349-201
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075979
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Metformin Hydrochloride Extended Release

Package NDC: 49349-201-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-201-02)

NDC Information of Metformin Hydrochloride Extended Release

NDC Code 49349-201-02
Proprietary Name Metformin Hydrochloride Extended Release
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-201-02)
Product NDC 49349-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride Extended Release
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride Extended Release


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