# Fosphenytoin Sodium

NDC: 65162-999
Generic name: Fosphenytoin Sodium
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20130517

FDA application: ANDA078476

## 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:"65162-999"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-999
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87ff8a91-5b37-401c-b75c-dc6efd348761