# Gabapentin

NDC: 71335-2037
Generic name: Gabapentin
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151101

FDA application: ANDA206402

## 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:"71335-2037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f31172a2-0ae9-49f2-b797-b26fe33f3f64