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Ropinirole Hydrochloride - 68382-339-10 - (Ropinirole Hydrochloride)

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Drug Information of Ropinirole Hydrochloride

Product NDC: 68382-339
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: 68382-339
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090411
Marketing Category: ANDA
Start Marketing Date: 20090923

Package Information of Ropinirole Hydrochloride

Package NDC: 68382-339-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (68382-339-10)

NDC Information of Ropinirole Hydrochloride

NDC Code 68382-339-10
Proprietary Name Ropinirole Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (68382-339-10)
Product NDC 68382-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090923
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
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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