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Metformin Hydrochloride - 43063-372-60 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 43063-372
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 750    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: 43063-372
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076869
Marketing Category: ANDA
Start Marketing Date: 20050412

Package Information of Metformin Hydrochloride

Package NDC: 43063-372-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-372-60)

NDC Information of Metformin Hydrochloride

NDC Code 43063-372-60
Proprietary Name Metformin Hydrochloride
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-372-60)
Product NDC 43063-372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050412
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


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