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METFORMIN HYDROCHLORIDE - 21695-473-78 - (METFORMIN HYDROCHLORIDE)

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Drug Information of METFORMIN HYDROCHLORIDE

Product NDC: 21695-473
Proprietary Name: METFORMIN HYDROCHLORIDE
Non Proprietary Name: METFORMIN HYDROCHLORIDE
Active Ingredient(s): 1000    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: 21695-473
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075967
Marketing Category: ANDA
Start Marketing Date: 20020129

Package Information of METFORMIN HYDROCHLORIDE

Package NDC: 21695-473-78
Package Description: 180 TABLET in 1 BOTTLE (21695-473-78)

NDC Information of METFORMIN HYDROCHLORIDE

NDC Code 21695-473-78
Proprietary Name METFORMIN HYDROCHLORIDE
Package Description 180 TABLET in 1 BOTTLE (21695-473-78)
Product NDC 21695-473
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020129
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of METFORMIN HYDROCHLORIDE


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