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Metformin Hydrochloride - 0093-7214-98 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 0093-7214
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 1000    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: 0093-7214
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075978
Marketing Category: ANDA
Start Marketing Date: 20030417

Package Information of Metformin Hydrochloride

Package NDC: 0093-7214-98
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0093-7214-98)

NDC Information of Metformin Hydrochloride

NDC Code 0093-7214-98
Proprietary Name Metformin Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0093-7214-98)
Product NDC 0093-7214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030417
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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