United States · FDA National Drug Code directory

VEOZAH

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
0469-2460_462f0a23-98d6-4154-b113-322008069743
Product NDC
0469-2460
Form
TABLET, FILM COATED
Composition / generic term
fezolinetant
Labeler
Astellas Pharma US, Inc.
Marketing category
NDA
Marketing start / end (source format)
20230516
Source listing expiry
20271231

Source-listed ingredients

  • FEZOLINETANT — 45 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 CARTON in 1 TRAY (0469-2460-28) / 1 BOTTLE in 1 CARTON (0469-2460-07) / 7 TABLET, FILM COATED in 1 BOTTLE · 0469-2460-28

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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