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Metformin Hydrochloride - 52125-400-20 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 52125-400
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 52125-400
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077095
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of Metformin Hydrochloride

Package NDC: 52125-400-20
Package Description: 100 TABLET, FILM COATED in 1 VIAL (52125-400-20)

NDC Information of Metformin Hydrochloride

NDC Code 52125-400-20
Proprietary Name Metformin Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 VIAL (52125-400-20)
Product NDC 52125-400
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130514
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


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