NDC 72786-101 – Oxbryta

Voxelotor 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72786-101

Product details

Brand name
Oxbryta
Generic name
Voxelotor
Labeler
Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA213137
Marketed since
November 25, 2019
Listing expires
December 31, 2026
Pharmacologic class
Hemoglobin S Polymerization Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Oxbryta →

Package NDC codes (1)

Package NDCDescriptionSince
72786-101-0190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-101-01)Nov 25, 2019

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