United States · FDA National Drug Code directory
Fosphenytoin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63323-403_84385df0-4793-47d2-8e49-5c84668a0ba3
- Product NDC
- 63323-403
- Form
- INJECTION, SOLUTION
- Composition / generic term
- FOSPHENYTOIN SODIUM
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091214
- Source listing expiry
- 20261231
Source-listed ingredients
- FOSPHENYTOIN SODIUM — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 TRAY (63323-403-02) / 2 mL in 1 VIAL (63323-403-01) · 63323-403-02
- 10 VIAL in 1 TRAY (63323-403-10) / 10 mL in 1 VIAL (63323-403-04) · 63323-403-10
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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