ropinirole

Product NDC
63629-6315
11-digit product format
636296315
Labeler code
63629
Product ID
63629-6315_477099be-4c6d-4e50-9183-80c6f6ae09f1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ropinirole
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090135
Marketing category
ANDA
Marketing start
2010-02-25
Marketing end
0000-00-00
Substance
ROPINIROLE HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-6315-12022-02-25C16284748780-19d75b9d0-3331-f424-e053-dadaa90a57ce1c4c5e09-5107-47c2-a070-3fa1917066f0
63629-6315-12020-01-31C16284748780-19d75b9d0-3331-f424-e053-dadaa90a57ce1c4c5e09-5107-47c2-a070-3fa1917066f0