# Gabapentin

NDC: 69434-044
Generic name: Gabapentin
Labeler / Manufacturer: Zhejiang Yongtai Pharmaceutical Co., Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20251203

FDA application: ANDA213603

## 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:"69434-044"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69434-044
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1eda6cc-d9b2-4df4-a09b-20eebded760f