# pramipexole dihydrochloride

NDC: 64380-751
Generic name: pramipexole dihydrochloride
Labeler / Manufacturer: Strides Pharma Science Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210215

FDA application: ANDA202702

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: 1.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64380-751"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64380-751
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fb2260d6-204c-4d25-a331-0f8340d83a6e