# Pregabalin

NDC: 71335-1822
Generic name: Pregabalin
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20191008

FDA application: ANDA206912

## Active ingredients

- PREGABALIN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-1822"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1822
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2d45d41-a787-4912-962d-0bd98b70d58a