# Neurontin

NDC: 0071-0401
Generic name: gabapentin
Labeler / Manufacturer: Parke-Davis Div of Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19981009
Marketing ended: 20260731
FDA application: NDA020882

## Active ingredients

- GABAPENTIN: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0071-0401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0071-0401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee9ad9ed-6d9f-4ee1-9d7f-cfad438df388