# Phenytoin

NDC: 51672-4069
Generic name: Phenytoin
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20040408

FDA application: ANDA040521

## Active ingredients

- PHENYTOIN: 125 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4069"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4069
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=093fd736-5971-47af-b4ef-08c1696cebe8