# ropinirole hydrochloride

NDC: 71335-0587
Generic name: ropinirole hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110920

FDA application: ANDA078110

## Active ingredients

- ROPINIROLE HYDROCHLORIDE: .25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-0587"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0587
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c10444a-48da-469d-bf8f-1e6e0b7e15f8