Home NDC 67296-2268 Ticagrelor
Product NDC 67296-2268
11-digit product format 672962268
Labeler code 67296
Product ID 67296-2268_5a66211c-c575-e6e6-e063-6294a90a0a79
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ticagrelor
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Redpharm Drug
Application ANDA208576
Marketing category ANDA
Marketing start 2025-05-01
Substance TICAGRELOR
Active strength 90 mg/1
Pharmacologic classes Cytochrome P450 3A4 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P-Glycoprotein Inhibitors [MoA], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A208576-001 TICAGRELOR TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 A208576-002 TICAGRELOR TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-10-15 13:18:30 2026-09 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 c2088c7a36db…2026-10-15 13:18:30 2026-09 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 c2088c7a36db…2026-09-14 22:38:34 2026-08 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 84e616aacf4f…2026-09-14 22:38:34 2026-08 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 84e616aacf4f…2026-08-18 06:07:40 2026-07 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 6a471c1ec25d…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A208576-001 TICAGRELOR 90MG TABLET / ORAL AB 2025-05-01 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A208576-002 TICAGRELOR 60MG TABLET / ORAL AB 2025-10-28 a50c72e98297…
Observed Orange Book normalized TE history# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ticagrelor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TICAGRELOR 90 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination GLH0314RVC Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1116635 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 67296-2268-2 67296226802 7 TABLET, FILM COATED in 1 BOTTLE (67296-2268-2) 2025-05-01 No No Current 67296-2268-6 67296226806 60 TABLET, FILM COATED in 1 BOTTLE (67296-2268-6) 2025-05-01 No No Current