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Metformin Hydrochloride Extended Release - 0904-5794-61 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride Extended Release

Product NDC: 0904-5794
Proprietary Name: Metformin Hydrochloride Extended Release
Non Proprietary Name: metformin hydrochloride
Active Ingredient(s): 500    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 Extended Release

Product NDC: 0904-5794
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076706
Marketing Category: ANDA
Start Marketing Date: 20090610

Package Information of Metformin Hydrochloride Extended Release

Package NDC: 0904-5794-61
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5794-61)

NDC Information of Metformin Hydrochloride Extended Release

NDC Code 0904-5794-61
Proprietary Name Metformin Hydrochloride Extended Release
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5794-61)
Product NDC 0904-5794
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090610
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride Extended Release


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