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
- 43598-480_505b2d2b-bc2d-41dd-9384-a90d3d4d91ec
- Product NDC
- 43598-480
- Form
- TABLET
- Composition / generic term
- Ticagrelor
- Labeler
- Dr. Reddys Laboratories Inc
- 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
- 180 TABLET in 1 BOTTLE (43598-480-18) · 43598-480-18
- 60 TABLET in 1 BOTTLE (43598-480-60) · 43598-480-60
- 10 BLISTER PACK in 1 CARTON (43598-480-78) / 10 TABLET in 1 BLISTER PACK · 43598-480-78
- 1 BLISTER PACK in 1 CARTON (43598-480-79) / 10 TABLET in 1 BLISTER PACK · 43598-480-79
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.
Browse United States records →