# Pregabalin

NDC: 27808-239
Generic name: Pregabalin
Labeler / Manufacturer: Tris Pharma Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210715

FDA application: ANDA214322

## Active ingredients

- PREGABALIN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62aa850d-199c-44d5-a730-45f43efa850e