# Pramipexole Dihydrochloride

NDC: 50228-131
Generic name: Pramipexole Dihydrochloride
Labeler / Manufacturer: ScieGen Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20141029

FDA application: ANDA203855

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: 1.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50228-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=395fee34-43dc-4840-a6b8-70d5736f9c8b