Ropinirole - 0054-0122-25 - (rOPINIRole)

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Drug Information of Ropinirole

Product NDC: 0054-0122
Proprietary Name: Ropinirole
Non Proprietary Name: rOPINIRole
Active Ingredient(s): 5    mg/1 & nbsp;   rOPINIRole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ropinirole

Product NDC: 0054-0122
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077852
Marketing Category: ANDA
Start Marketing Date: 20080505

Package Information of Ropinirole

Package NDC: 0054-0122-25
Package Description: 100 TABLET in 1 BOTTLE (0054-0122-25)

NDC Information of Ropinirole

NDC Code 0054-0122-25
Proprietary Name Ropinirole
Package Description 100 TABLET in 1 BOTTLE (0054-0122-25)
Product NDC 0054-0122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rOPINIRole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080505
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, 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


General Information