# Gabapentin

NDC: 64380-727
Generic name: Gabapentin
Labeler / Manufacturer: Strides Pharma Science Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251110

FDA application: ANDA203244

## 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:"64380-727"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64380-727
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bec31452-b52b-4698-ba4c-0b614780ee84