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
- 71610-914_4887c1b7-be57-6eb9-e063-6294a90ab88d
- Product NDC
- 71610-914
- Form
- TABLET, FILM COATED
- Composition / generic term
- TICAGRELOR
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250507
- Source listing expiry
- 20271231
Source-listed ingredients
- TICAGRELOR — 90 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5400 TABLET, FILM COATED in 1 BOTTLE (71610-914-41) · 71610-914-41
- 1800 TABLET, FILM COATED in 1 BOTTLE (71610-914-42) · 71610-914-42
Source and coverage
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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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