# GABAPENTIN

NDC: 76282-321
Generic name: GABAPENTIN
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20100426

FDA application: ANDA090705

## 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:"76282-321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41d1ead3-046e-4abf-ae0a-cb126a1f5848