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Metformin Hydrochloride - 0904-6108-60 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 0904-6108
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 750    mg/1 & nbsp;   Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 0904-6108
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078596
Marketing Category: ANDA
Start Marketing Date: 20100510

Package Information of Metformin Hydrochloride

Package NDC: 0904-6108-60
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0904-6108-60)

NDC Information of Metformin Hydrochloride

NDC Code 0904-6108-60
Proprietary Name Metformin Hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0904-6108-60)
Product NDC 0904-6108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100510
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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