United States · FDA National Drug Code directory
Phenytoin 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
- 0641-2555_1b68e42c-ebb1-4798-adba-712a41cd1cf4
- Product NDC
- 0641-2555
- Form
- INJECTION
- Composition / generic term
- Phenytoin Sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19750716
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYTOIN SODIUM — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (0641-2555-10) / 5 mL in 1 VIAL (0641-2555-41) · 0641-2555-10
- 25 VIAL in 1 CARTON (0641-2555-45) / 5 mL in 1 VIAL (0641-2555-41) · 0641-2555-45
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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