United States · FDA National Drug Code directory

CX-038839 OMICRON (XBB.1.5)

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
50024-100_312cf34c-e226-eabf-e063-6294a90a711c
Product NDC
50024-100
Form
INJECTION, SUSPENSION
Composition / generic term
CX-038839 OMICRON (XBB.1.5)
Labeler
ROVI Pharma Industrial Services S.A.
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing start / end (source format)
20230911
Source listing expiry
20261231

Source-listed ingredients

  • CX-038839 OMICRON (XBB.1.5) — 50 ug/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 SYRINGE, PLASTIC in 1 CARTON (50024-100-01) / .5 mL in 1 SYRINGE, PLASTIC (50024-100-00) · 50024-100-01

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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