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Metformin Hydrochloride - 60429-280-01 - (Metformin Hydrochloride ER)

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Drug Information of Metformin Hydrochloride

Product NDC: 60429-280
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride ER
Active Ingredient(s): 750    mg/1 & nbsp;   Metformin Hydrochloride ER
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 60429-280
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076869
Marketing Category: ANDA
Start Marketing Date: 20060412

Package Information of Metformin Hydrochloride

Package NDC: 60429-280-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60429-280-01)

NDC Information of Metformin Hydrochloride

NDC Code 60429-280-01
Proprietary Name Metformin Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60429-280-01)
Product NDC 60429-280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride ER
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060412
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


General Information