# ropinirole hydrochloride

NDC: 43547-271
Generic name: ropinirole hydrochloride
Labeler / Manufacturer: SOLCO HEALTHCARE US, LLC
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: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43547-271"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43547-271
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7734ef0b-584f-42dd-a8b5-adbdf4e4df93