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Metformin Hydrochloride - 0904-6091-61 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 0904-6091
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
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 0904-6091
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20100111

Package Information of Metformin Hydrochloride

Package NDC: 0904-6091-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-6091-61)

NDC Information of Metformin Hydrochloride

NDC Code 0904-6091-61
Proprietary Name Metformin Hydrochloride
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-6091-61)
Product NDC 0904-6091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100111
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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