Ropinirole Hydrochloride

Product NDC
63629-4977
11-digit product format
636294977
Labeler code
63629
Product ID
63629-4977_88db5bac-73c7-4b4f-a207-8f895223d778
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ropinirole Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090429
Marketing category
ANDA
Marketing start
2009-09-18
Marketing end
0000-00-00
Substance
ROPINIROLE HYDROCHLORIDE
Active strength
0 mg/1
Pharmacologic classes
Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#