# Pregabalin

NDC: 69367-424
Generic name: Pregabalin
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20251117

FDA application: ANDA212988

## Active ingredients

- PREGABALIN: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-424"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-424
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6b0ee2cf-52c3-4052-bea0-1458a4233745