# Fosphenytoin Sodium

NDC: 0143-9788
Generic name: Fosphenytoin Sodium
Labeler / Manufacturer: West-Ward Pharmaceuticals Corp
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20091202

FDA application: ANDA078765

## Active ingredients

- FOSPHENYTOIN SODIUM: 50 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9788"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9788
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c92df63b-5140-4213-8d43-8327ff6230b7