United States · FDA National Drug Code directory
YESINTEK
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
- 83257-024_326c6710-ed89-ec68-64de-c829281376d4
- Product NDC
- 83257-024
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ustekinumab
- Labeler
- Biocon Biologics Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 20250222
- Source listing expiry
- 20271231
Source-listed ingredients
- USTEKINUMAB — 45 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-USE in 1 CARTON (83257-024-11) / .5 mL in 1 VIAL, SINGLE-USE · 83257-024-11
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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