# Pramipexole Dihydrochloride

NDC: 57237-182
Generic name: Pramipexole Dihydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20121026

FDA application: ANDA202633

## 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:"57237-182"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-182
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56e8d1f6-6dbf-4e11-a177-a56bbfb9f8ec