# Ropinirole

NDC: 69452-362
Generic name: Ropinirole
Labeler / Manufacturer: Bionpharma 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: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-362"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-362
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4e6b070c-50a6-4742-af3c-59b45c45735e