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METFORMIN HYDROCHLORIDE - 60760-042-60 - (METFORMIN HYDROCHLORIDE)

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Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 60760-042
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: 60760-042
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077336
Marketing Category: ANDA
Start Marketing Date: 20060209

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 60760-042-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-042-60)

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 60760-042-60
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-042-60)
Product NDC 60760-042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060209
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
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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