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Metformin Hydrochloride - 54868-5505-1 - (metformin hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 54868-5505
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: 54868-5505
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077336
Marketing Category: ANDA
Start Marketing Date: 20060117

Package Information of Metformin Hydrochloride

Package NDC: 54868-5505-1
Package Description: 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5505-1)

NDC Information of Metformin Hydrochloride

NDC Code 54868-5505-1
Proprietary Name Metformin Hydrochloride
Package Description 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5505-1)
Product NDC 54868-5505
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060117
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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