# Gabapentin

NDC: 69097-812
Generic name: Gabapentin
Labeler / Manufacturer: Cipla USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160722

FDA application: ANDA202764

## Active ingredients

- GABAPENTIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69097-812"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-812
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c3ac86f-b8f7-42bf-942a-db854d946e54