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#