# Pregabalin

NDC: 80425-0025
Generic name: Pregabalin
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190719

FDA application: ANDA209743

## Active ingredients

- PREGABALIN: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0025"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0025
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af739a0d-a3cd-754f-e053-2a95a90ad655