# ROPINIROLE

NDC: 67046-1489
Generic name: ROPINIROLE
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250129

FDA application: ANDA090429

## Active ingredients

- ROPINIROLE HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67046-1489"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-1489
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2cdae415-479b-c14c-e063-6394a90adb6c