# Gabapentin

NDC: 69367-343
Generic name: Gabapentin
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20211101

FDA application: ANDA075477

## 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:"69367-343"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-343
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ad96553-73a4-4a9b-8a89-10a29b794ed3