# Pramipexole Dihydrochloride

NDC: 46708-005
Generic name: Pramipexole Dihydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160322

FDA application: ANDA078894

## Active ingredients

- PRAMIPEXOLE DIHYDROCHLORIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92f6ef1e-3256-45a7-a409-80dd85e95187