# Ropinirole

NDC: 87063-201
Generic name: Ropinirole
Labeler / Manufacturer: ASCLEMED USA INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220915

FDA application: ANDA079229

## 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:"87063-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87063-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f3612f0-0976-4de7-a1d6-eabaa8b75f9c