# ropinirole hydrochloride

NDC: 60687-577
Generic name: ropinirole hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210610

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:"60687-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6849b3c0-e36b-4bea-82f2-b33ae3d44c95