United States · FDA National Drug Code directory
Skyrizi
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
- 0074-4059_388f783d-f41e-4f04-bf64-ec637fe05bdf
- Product NDC
- 0074-4059
- Form
- INJECTION, SOLUTION
- Composition / generic term
- risankizumab-rzaa
- Labeler
- AbbVie Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 20260612
- Source listing expiry
- 20271231
Source-listed ingredients
- RISANKIZUMAB — 55 mg/.37mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 SYRINGE, GLASS in 1 CARTON (0074-4059-01) / .37 mL in 1 SYRINGE, GLASS · 0074-4059-01
- 1 SYRINGE, GLASS in 1 CARTON (0074-4059-71) / .37 mL in 1 SYRINGE, GLASS · 0074-4059-71
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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