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METFORMIN HYDROCHLORIDE - 16590-397-30 - (METFORMIN HYDROCHLORIDE)

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Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 16590-397
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: 16590-397
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077064
Marketing Category: ANDA
Start Marketing Date: 20050928

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 16590-397-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-397-30)

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 16590-397-30
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-397-30)
Product NDC 16590-397
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 STAT Rx USA LLC
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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