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Metformin Hydrochloride - 62037-571-05 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 62037-571
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 62037-571
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076172
Marketing Category: ANDA
Start Marketing Date: 20040616

Package Information of Metformin Hydrochloride

Package NDC: 62037-571-05
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-571-05)

NDC Information of Metformin Hydrochloride

NDC Code 62037-571-05
Proprietary Name Metformin Hydrochloride
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-571-05)
Product NDC 62037-571
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040616
Marketing Category Name ANDA
Labeler Name Watson Pharma, 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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