Home > National Drug Code (NDC) > METFORMIN HYDROCHLORIDE

METFORMIN HYDROCHLORIDE - 68382-029-30 - (METFORMIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 68382-029
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: 68382-029
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077064
Marketing Category: ANDA
Start Marketing Date: 20050928

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 68382-029-30
Package Description: 10 BLISTER PACK in 1 CARTON (68382-029-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 68382-029-30
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 10 BLISTER PACK in 1 CARTON (68382-029-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 68382-029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050928
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of METFORMIN HYDROCHLORIDE


General Information