# Gabapentin

NDC: 80425-0031
Generic name: Gabapentin
Labeler / Manufacturer: ADVANCED RX OF TENNESSEE, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180514

FDA application: ANDA206943

## Active ingredients

- GABAPENTIN: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af73fbd8-9731-e6bf-e053-2995a90af65d