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
67877-491_d7f89cc8-6226-4caa-b8ee-22155683489c
Product NDC
67877-491
Form
TABLET
Composition / generic term
Ticagrelor
Labeler
Ascend Laboratories, LLC
Marketing category
ANDA
Marketing start / end (source format)
20250430
Source listing expiry
20271231

Source-listed ingredients

  • TICAGRELOR — 90 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 TABLET in 1 BOTTLE (67877-491-05) · 67877-491-05
  • 60 TABLET in 1 BOTTLE (67877-491-60) · 67877-491-60

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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