# Pramipexole dihydrochloride

NDC: 50742-331
Generic name: Pramipexole dihydrochloride
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220310

FDA application: ANDA213444

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: .375 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-331"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-331
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d2b1d2c-ae22-424a-bad7-ce24a817b042