United States · FDA National Drug Code directory

Tafinlar

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
0078-1154_6c546993-1f7f-409b-b108-60f22e9b948a
Product NDC
0078-1154
Form
TABLET, FOR SUSPENSION
Composition / generic term
dabrafenib
Labeler
Novartis Pharmaceuticals Corporation
Marketing category
NDA
Marketing start / end (source format)
20230316
Source listing expiry
20271231

Source-listed ingredients

  • DABRAFENIB MESYLATE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 210 TABLET, FOR SUSPENSION in 1 BOTTLE (0078-1154-21) · 0078-1154-21

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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