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ROPINIROLE HYDROCHLORIDE - 64720-202-10 - (ROPINIROLE HYDROCHLORIDE)

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Drug Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 64720-202
Proprietary Name: ROPINIROLE HYDROCHLORIDE
Non Proprietary Name: ROPINIROLE HYDROCHLORIDE
Active Ingredient(s): .5    mg/1 & nbsp;   ROPINIROLE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 64720-202
Labeler Name: Corepharma LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078230
Marketing Category: ANDA
Start Marketing Date: 20080521

Package Information of ROPINIROLE HYDROCHLORIDE

Package NDC: 64720-202-10
Package Description: 100 TABLET, COATED in 1 BOTTLE, PLASTIC (64720-202-10)

NDC Information of ROPINIROLE HYDROCHLORIDE

NDC Code 64720-202-10
Proprietary Name ROPINIROLE HYDROCHLORIDE
Package Description 100 TABLET, COATED in 1 BOTTLE, PLASTIC (64720-202-10)
Product NDC 64720-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPINIROLE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20080521
Marketing Category Name ANDA
Labeler Name Corepharma LLC.
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of ROPINIROLE HYDROCHLORIDE


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