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Ropinirole Hydrochloride - 64220-421-01 - (Ropinirole Hydrochloride)

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Drug Information of Ropinirole Hydrochloride

Product NDC: 64220-421
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ropinirole Hydrochloride

Product NDC: 64220-421
Labeler Name: Zhejiang Huahai Pharmaceutical Co., Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078110
Marketing Category: ANDA
Start Marketing Date: 20110810

Package Information of Ropinirole Hydrochloride

Package NDC: 64220-421-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (64220-421-01)

NDC Information of Ropinirole Hydrochloride

NDC Code 64220-421-01
Proprietary Name Ropinirole Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (64220-421-01)
Product NDC 64220-421
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110810
Marketing Category Name ANDA
Labeler Name Zhejiang Huahai Pharmaceutical Co., Ltd.
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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