# Pregabalin

NDC: 72888-050
Generic name: Pregabalin
Labeler / Manufacturer: Advagen Pharma Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220322

FDA application: ANDA215249

## Active ingredients

- PREGABALIN: 165 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72888-050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72888-050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2ffee7e7-bfa0-4933-9baf-7df55080816e