# Neurontin

NDC: 58151-285
Generic name: gabapentin
Labeler / Manufacturer: Viatris Specialty LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250919

FDA application: NDA020882

## Active ingredients

- GABAPENTIN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58151-285"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58151-285
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97935fd9-1d4a-43b6-a5d9-de994591187b