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Metformin Hydrochloride - 25000-134-14 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 25000-134
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 500    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: 25000-134
Labeler Name: MARKSANS PHARMA LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090888
Marketing Category: ANDA
Start Marketing Date: 20120601

Package Information of Metformin Hydrochloride

Package NDC: 25000-134-14
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (25000-134-14)

NDC Information of Metformin Hydrochloride

NDC Code 25000-134-14
Proprietary Name Metformin Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (25000-134-14)
Product NDC 25000-134
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120601
Marketing Category Name ANDA
Labeler Name MARKSANS PHARMA LIMITED
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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