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Metformin Hydrochloride - 65862-292-30 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 65862-292
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 750    mg/1 & nbsp;   Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 65862-292
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079118
Marketing Category: ANDA
Start Marketing Date: 20120720

Package Information of Metformin Hydrochloride

Package NDC: 65862-292-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65862-292-30)

NDC Information of Metformin Hydrochloride

NDC Code 65862-292-30
Proprietary Name Metformin Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65862-292-30)
Product NDC 65862-292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120720
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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