# Pramipexole dihydrochloride

NDC: 68462-334
Generic name: Pramipexole dihydrochloride
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20101008

FDA application: ANDA090781

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: 1.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-334"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-334
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44c336d2-01d1-4f13-bad9-549cdc3505ec