# Phenytoin Sodium

NDC: 29300-379
Generic name: Phenytoin Sodium
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20221112

FDA application: ANDA213834

## Active ingredients

- PHENYTOIN SODIUM: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-379"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-379
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=afdf66e0-5f99-444e-bc06-2fdddc507f5c