# ropinirole hydrochloride

NDC: 50090-1330
Generic name: ropinirole hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-1330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-1330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c4dacc6-cebc-4f42-85fc-41083512b290