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Metformin Hydrochloride - 65862-008-50 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 65862-008
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 500    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: 65862-008
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077095
Marketing Category: ANDA
Start Marketing Date: 20050114

Package Information of Metformin Hydrochloride

Package NDC: 65862-008-50
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (65862-008-50)

NDC Information of Metformin Hydrochloride

NDC Code 65862-008-50
Proprietary Name Metformin Hydrochloride
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (65862-008-50)
Product NDC 65862-008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050114
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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