# Pramipexole dihydrochloride

NDC: 33342-034
Generic name: Pramipexole dihydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120921

FDA application: ANDA202164

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-034"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-034
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8c94917-73a1-44c2-8fd8-07f45054176b