United States · FDA National Drug Code directory

TICAGRELOR

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
50268-826_42501349-0107-5655-e063-6394a90a9b0c
Product NDC
50268-826
Form
TABLET
Composition / generic term
TICAGRELOR
Labeler
AvPAK
Marketing category
ANDA
Marketing start / end (source format)
20251029
Source listing expiry
20261231

Source-listed ingredients

  • TICAGRELOR — 90 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 BOX (50268-826-01) / 1 TABLET in 1 BLISTER PACK (50268-826-11) · 50268-826-01

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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