# Gabapentin

NDC: 63739-902
Generic name: Gabapentin
Labeler / Manufacturer: McKesson Corporation dba Sky Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210715

FDA application: ANDA090858

## Active ingredients

- GABAPENTIN: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63739-902"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-902
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=23eb133e-2f74-4219-9892-0a8e770ec032