# Fosphenytoin sodium

NDC: 68462-622
Generic name: Fosphenytoin sodium
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20231013

FDA application: ANDA214926

## 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:"68462-622"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-622
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0def32c-e693-43e5-9509-0cef9642441c