# Pregabalin

NDC: 29300-445
Generic name: Pregabalin
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260803

FDA application: ANDA219593

## Active ingredients

- PREGABALIN: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-445"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-445
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=284f2c15-24ef-466b-8110-3c2e87483509