# Pramipexole Dihydrochloride

NDC: 60687-581
Generic name: Pramipexole Dihydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200813

FDA application: ANDA090865

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-581"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-581
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4d97c2e-f447-4cfe-b9d4-852323f0cfb5