United States · FDA National Drug Code directory
Fosphenytoin Sodium
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
- 0641-6136_d276be92-654c-4912-8dc5-3e148c835523
- Product NDC
- 0641-6136
- Form
- INJECTION
- Composition / generic term
- Fosphenytoin Sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070806
- 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 CARTON (0641-6136-25) / 2 mL in 1 VIAL (0641-6136-01) · 0641-6136-25
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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