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Metformin Hydrochloride - 65162-174-11 - (Metformin)

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Drug Information of Metformin Hydrochloride

Product NDC: 65162-174
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin
Active Ingredient(s): 850    mg/1 & nbsp;   Metformin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 65162-174
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Metformin Hydrochloride

Package NDC: 65162-174-11
Package Description: 1000 TABLET in 1 BOTTLE (65162-174-11)

NDC Information of Metformin Hydrochloride

NDC Code 65162-174-11
Proprietary Name Metformin Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (65162-174-11)
Product NDC 65162-174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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