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Metformin Hydrochloride - 43063-012-93 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 43063-012
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: 43063-012
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20120427

Package Information of Metformin Hydrochloride

Package NDC: 43063-012-93
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (43063-012-93)

NDC Information of Metformin Hydrochloride

NDC Code 43063-012-93
Proprietary Name Metformin Hydrochloride
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (43063-012-93)
Product NDC 43063-012
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 PD-Rx Pharmaceuticals, 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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