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#