# Gabapentin

NDC: 70518-1469
Generic name: Gabapentin
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20181005

FDA application: ANDA090858

## Active ingredients

- GABAPENTIN: 400 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1469"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1469
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=78445dbf-c7cd-419f-a7be-72821e496628