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METFORMIN HYDROCHLORIDE - 67046-462-30 - (METFORMIN HYDROCHLORIDE)

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Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 67046-462
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: 67046-462
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077064
Marketing Category: ANDA
Start Marketing Date: 20100729

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 67046-462-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-462-30)

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 67046-462-30
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-462-30)
Product NDC 67046-462
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100729
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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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