# ropinirole

NDC: 16729-232
Generic name: ropinirole
Labeler / Manufacturer: Accord Healthcare Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181017

FDA application: ANDA204022

## Active ingredients

- ROPINIROLE HYDROCHLORIDE: .25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16729-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16729-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a2a5b63-5b14-6975-e054-00144ff8d46c