# Pregabalin

NDC: 47335-691
Generic name: Pregabalin
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20191204

FDA application: ANDA091157

## Active ingredients

- PREGABALIN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-691"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-691
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee7b9119-e88f-48ad-ae97-55e53374e62f