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Metformin Hydrochloride - 13668-013-12 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 13668-013
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: 13668-013
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079226
Marketing Category: ANDA
Start Marketing Date: 20100218

Package Information of Metformin Hydrochloride

Package NDC: 13668-013-12
Package Description: 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-013-12)

NDC Information of Metformin Hydrochloride

NDC Code 13668-013-12
Proprietary Name Metformin Hydrochloride
Package Description 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-013-12)
Product NDC 13668-013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100218
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
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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