United States · FDA National Drug Code directory

TYKERB

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
0078-0671_940eccaf-92b4-4562-8579-24a53c1bc48d
Product NDC
0078-0671
Form
TABLET
Composition / generic term
lapatinib
Labeler
Novartis Pharmaceuticals Corporation
Marketing category
NDA
Marketing start / end (source format)
20160803
Source listing expiry
20271231

Source-listed ingredients

  • LAPATINIB DITOSYLATE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 150 TABLET in 1 BOTTLE (0078-0671-19) · 0078-0671-19

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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