# Gabapentin

NDC: 63187-148
Generic name: Gabapentin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20111006

FDA application: ANDA200651

## Active ingredients

- GABAPENTIN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c79d94ec-117d-4fb6-845d-1954e3472bb0