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Metformin Hydrochloride - 60505-0191-4 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 60505-0191
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: metformin hydrochloride
Active Ingredient(s): 850    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: 60505-0191
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075984
Marketing Category: ANDA
Start Marketing Date: 20040301

Package Information of Metformin Hydrochloride

Package NDC: 60505-0191-4
Package Description: 2500 TABLET, FILM COATED in 1 BOTTLE (60505-0191-4)

NDC Information of Metformin Hydrochloride

NDC Code 60505-0191-4
Proprietary Name Metformin Hydrochloride
Package Description 2500 TABLET, FILM COATED in 1 BOTTLE (60505-0191-4)
Product NDC 60505-0191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040301
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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