# Gabapentin

NDC: 60687-507
Generic name: Gabapentin
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200324

FDA application: ANDA078926

## Active ingredients

- GABAPENTIN: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-507"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-507
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=765c7ce0-bbf5-4265-8ff0-1ba092c69865