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Metformin Hydrochloride - 65162-220-10 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 65162-220
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
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 65162-220
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20120427

Package Information of Metformin Hydrochloride

Package NDC: 65162-220-10
Package Description: 100 TABLET in 1 BOTTLE (65162-220-10)

NDC Information of Metformin Hydrochloride

NDC Code 65162-220-10
Proprietary Name Metformin Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (65162-220-10)
Product NDC 65162-220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120427
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
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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