# Gabapentin

NDC: 73352-231
Generic name: Gabapentin
Labeler / Manufacturer: Trifluent Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260817

FDA application: ANDA204989

## Active ingredients

- GABAPENTIN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73352-231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73352-231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=59442de1-7cf0-35f6-e063-6294a90a57d7