# Gabapentin

NDC: 85509-2180
Generic name: Gabapentin
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160218

FDA application: ANDA204989

## Active ingredients

- GABAPENTIN: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-2180"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-2180
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f95c01f-200e-bfd7-e063-6394a90abc38