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metformin hydrochloride - 0185-4416-01 - (metformin hydrochloride)

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Drug Information of metformin hydrochloride

Product NDC: 0185-4416
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: 0185-4416
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076873
Marketing Category: ANDA
Start Marketing Date: 20041214

Package Information of metformin hydrochloride

Package NDC: 0185-4416-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-4416-01)

NDC Information of metformin hydrochloride

NDC Code 0185-4416-01
Proprietary Name metformin hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-4416-01)
Product NDC 0185-4416
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041214
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
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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