# Gabapentin

NDC: 68001-412
Generic name: Gabapentin
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190930

FDA application: ANDA077662

## 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:"68001-412"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-412
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3368bf70-d466-4765-b2b7-7fe967a8c2b7