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metformin hydrochloride - 0185-0215-05 - (metformin hydrochloride)

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Drug Information of metformin hydrochloride

Product NDC: 0185-0215
Proprietary Name: metformin hydrochloride
Non Proprietary Name: metformin hydrochloride
Active Ingredient(s): 850    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: 0185-0215
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075965
Marketing Category: ANDA
Start Marketing Date: 20020125

Package Information of metformin hydrochloride

Package NDC: 0185-0215-05
Package Description: 500 TABLET in 1 BOTTLE (0185-0215-05)

NDC Information of metformin hydrochloride

NDC Code 0185-0215-05
Proprietary Name metformin hydrochloride
Package Description 500 TABLET in 1 BOTTLE (0185-0215-05)
Product NDC 0185-0215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020125
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of metformin hydrochloride


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