United States · FDA National Drug Code directory

Ayvakit

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
72064-120_beacc534-14e1-4fd2-978f-5646edd537f0
Product NDC
72064-120
Form
TABLET, FILM COATED
Composition / generic term
avapritinib
Labeler
Blueprint Medicines Corporation
Marketing category
NDA
Marketing start / end (source format)
20200109
Source listing expiry
20271231

Source-listed ingredients

  • AVAPRITINIB — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72064-120-30) · 72064-120-30

Source and coverage

Open FDA National Drug Code directory

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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