# Gabapentin

NDC: 71335-2701
Generic name: Gabapentin
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20111006

FDA application: ANDA200651

## Active ingredients

- GABAPENTIN: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f982b95-4e84-4e0c-a543-747bc3dd7531