United States · FDA National Drug Code directory

ustekinumab

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
57894-444_2e2c7c8d-c54a-43c7-bbb9-8aeb40088a06
Product NDC
57894-444
Form
SOLUTION
Composition / generic term
ustekinumab
Labeler
Janssen Biotech, Inc.
Marketing category
BLA
Marketing start / end (source format)
20250401
Source listing expiry
20271231

Source-listed ingredients

  • USTEKINUMAB — 130 mg/26mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-USE in 1 BOX (57894-444-01) / 26 mL in 1 VIAL, SINGLE-USE · 57894-444-01

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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