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Metformin Hydrochloride - 0615-5583-31 - (Metformin Hydrochloride)

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Drug Information of Metformin Hydrochloride

Product NDC: 0615-5583
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: 0615-5583
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076269
Marketing Category: ANDA
Start Marketing Date: 20100611

Package Information of Metformin Hydrochloride

Package NDC: 0615-5583-31
Package Description: 31 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-5583-31)

NDC Information of Metformin Hydrochloride

NDC Code 0615-5583-31
Proprietary Name Metformin Hydrochloride
Package Description 31 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-5583-31)
Product NDC 0615-5583
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100611
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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