# Pregabalin

NDC: 68788-7520
Generic name: PREGABALIN
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190719

FDA application: ANDA208677

## Active ingredients

- PREGABALIN: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7520"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7520
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce1419bc-c348-4407-b320-e0598d5a7b19