ropinirole - 0781-5786-31 - (ropinirole)

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Drug Information of ropinirole

Product NDC: 0781-5786
Proprietary Name: ropinirole
Non Proprietary Name: ropinirole
Active Ingredient(s): 8    mg/1 & nbsp;   ropinirole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ropinirole

Product NDC: 0781-5786
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201047
Marketing Category: ANDA
Start Marketing Date: 20120606

Package Information of ropinirole

Package NDC: 0781-5786-31
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5786-31)

NDC Information of ropinirole

NDC Code 0781-5786-31
Proprietary Name ropinirole
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5786-31)
Product NDC 0781-5786
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ropinirole
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120606
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of ropinirole


General Information