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Metformin Hydrochloride - 51079-995-20 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 51079-995
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: 51079-995
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075976
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of Metformin Hydrochloride

Package NDC: 51079-995-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-995-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-995-01)

NDC Information of Metformin Hydrochloride

NDC Code 51079-995-20
Proprietary Name Metformin Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-995-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-995-01)
Product NDC 51079-995
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111006
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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