# CEREBYX

NDC: 0069-6001
Generic name: Fosphenytoin Sodium
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20131028

FDA application: NDA020450

## Active ingredients

- FOSPHENYTOIN SODIUM: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0069-6001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-6001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4c36fad-0ba2-4cd4-9c5e-dcf843f38a5a