United States · FDA National Drug Code directory

TAZVERIK

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
72607-100_c4bd8d8a-22c1-4911-a9b4-7368582d8e5d
Product NDC
72607-100
Form
TABLET, FILM COATED
Composition / generic term
tazemetostat
Labeler
Epizyme, Inc.
Marketing category
NDA
Marketing start / end (source format)
20200123 / 20290430

Source-listed ingredients

  • TAZEMETOSTAT HYDROBROMIDE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 240 TABLET, FILM COATED in 1 BOTTLE (72607-100-00) · 72607-100-00

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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