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Metformin Hydrochloride - 43063-430-90 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 43063-430
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: 43063-430
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: 43063-430-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-430-90)

NDC Information of Metformin Hydrochloride

NDC Code 43063-430-90
Proprietary Name Metformin Hydrochloride
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-430-90)
Product NDC 43063-430
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 1000
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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