United States · FDA National Drug Code directory

OXBRYTA

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
72786-102_e27a3e07-438e-49d3-aae3-095e9379c7b4
Product NDC
72786-102
Form
TABLET, FILM COATED
Composition / generic term
Voxelotor
Labeler
Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.
Marketing category
NDA
Marketing start / end (source format)
20191125
Source listing expiry
20261231

Source-listed ingredients

  • VOXELOTOR — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-102-02) · 72786-102-02
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-102-03) · 72786-102-03

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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