# Ropinirole

NDC: 10135-675
Generic name: ropinirole
Labeler / Manufacturer: Marlex Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190315

FDA application: ANDA079165

## Active ingredients

- ROPINIROLE HYDROCHLORIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10135-675"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10135-675
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35d90f6f-3116-4afa-be2d-b65c160e8ab3