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METFORMIN HYDROCHLORIDE - 49349-847-20 - (METFORMIN HYDROCHLORIDE)

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Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 49349-847
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: 49349-847
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075967
Marketing Category: ANDA
Start Marketing Date: 20130530

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 49349-847-20
Package Description: 1000 TABLET in 1 VIAL (49349-847-20)

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 49349-847-20
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 1000 TABLET in 1 VIAL (49349-847-20)
Product NDC 49349-847
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130530
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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