United States · FDA National Drug Code directory

CEREBYX

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
0069-6001_c2767f24-e5ac-4d94-8bff-faf0a6eaf7c4
Product NDC
0069-6001
Form
INJECTION, SOLUTION
Composition / generic term
Fosphenytoin Sodium
Labeler
Pfizer Laboratories Div Pfizer Inc
Marketing category
NDA
Marketing start / end (source format)
20131028
Source listing expiry
20261231

Source-listed ingredients

  • FOSPHENYTOIN SODIUM — 50 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL in 1 PACKAGE (0069-6001-21) / 10 mL in 1 VIAL (0069-6001-10) · 0069-6001-21
  • 25 VIAL in 1 CARTON (0069-6001-25) / 2 mL in 1 VIAL (0069-6001-02) · 0069-6001-25

Source and coverage

Open FDA National Drug Code directory

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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CEREBYX — United States | Molindra Medicines