# Dilantin-125

NDC: 58151-115
Generic name: Phenytoin
Labeler / Manufacturer: Viatris Specialty LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20240419

FDA application: NDA008762

## 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:"58151-115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58151-115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f339f9e4-b289-4efe-82b9-46c57d1dc277