# Ropinirole

NDC: 64850-252
Generic name: Ropinirole
Labeler / Manufacturer: Elite Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20251110

FDA application: ANDA217862

## Active ingredients

- ROPINIROLE HYDROCHLORIDE: 6 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64850-252"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64850-252
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=307411be-1c4e-44f7-b94d-737a3384c107