# Gabapentin

NDC: 71205-064
Generic name: Gabapentin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20140403

FDA application: ANDA075350

## Active ingredients

- GABAPENTIN: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-064"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-064
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7cb37f9-e1df-4e2a-bde5-9bfa0e040d7a