# Pramipexole Dihydrochloride

NDC: 33342-211
Generic name: Pramipexole Dihydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200824

FDA application: ANDA206156

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: 2.25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-211"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-211
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1dbb8d2f-e0d9-4f8b-89d2-2a03496ef7be