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Ropinirole Hydrochloride - 64679-774-04 - (Ropinirole Hydrochloride)

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Drug Information of Ropinirole Hydrochloride

Product NDC: 64679-774
Proprietary Name: Ropinirole Hydrochloride
Non Proprietary Name: Ropinirole Hydrochloride
Active Ingredient(s): 8    mg/1 & nbsp;   Ropinirole Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ropinirole Hydrochloride

Product NDC: 64679-774
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091395
Marketing Category: ANDA
Start Marketing Date: 20120815

Package Information of Ropinirole Hydrochloride

Package NDC: 64679-774-04
Package Description: 10 BLISTER PACK in 1 CARTON (64679-774-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Ropinirole Hydrochloride

NDC Code 64679-774-04
Proprietary Name Ropinirole Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (64679-774-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 64679-774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole Hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120815
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Ropinirole Hydrochloride


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