# Gabapentin

NDC: 70518-2323
Generic name: Gabapentin
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190924

FDA application: ANDA200651

## Active ingredients

- GABAPENTIN: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2323"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2323
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=429a1bb5-babf-4f36-8264-46d71164f1c0