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Metformin Hydrochloride - 42291-605-10 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 42291-605
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
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 42291-605
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20120626

Package Information of Metformin Hydrochloride

Package NDC: 42291-605-10
Package Description: 1000 TABLET in 1 BOTTLE (42291-605-10)

NDC Information of Metformin Hydrochloride

NDC Code 42291-605-10
Proprietary Name Metformin Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (42291-605-10)
Product NDC 42291-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120626
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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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