United States · FDA National Drug Code directory
IMULDOSA
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
- 69448-019_be75347b-ab5d-4104-b90e-7c7b1f46fbef
- Product NDC
- 69448-019
- Form
- INJECTION
- Composition / generic term
- ustekinumab-srlf
- Labeler
- Accord BioPharma Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 20241018
- Source listing expiry
- 20271231
Source-listed ingredients
- USTEKINUMAB-SRLF — 130 mg/26mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-USE in 1 CARTON (69448-019-26) / 26 mL in 1 VIAL, SINGLE-USE · 69448-019-26
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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