# Pregabalin

NDC: 71610-618
Generic name: PREGABALIN
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190719

FDA application: ANDA208677

## Active ingredients

- PREGABALIN: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-618"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-618
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aa55a53c-96f6-4e0a-8b1d-e9d36e6ef2ec