NDC 55154-9618
Brilinta 90 mg tablet
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from AstraZeneca Pharmaceuticals LP's NDC 0186-0777.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants AstraZeneca Pharmaceuticals LP names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: MP0138 - May 25, 2017 · Class I · AstraZeneca Pharmaceuticals, LP
Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count professional sample bottle labeled as BRILINTA 90 mg tablets contained 5 ZURAMPIC 200 mg tablets, in addition to the expected 8 BRILINTA tablets.
Lots: Lot # JB5047, Exp 10/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ticagrelor: every company that makes it
- Form
- tablet, oral
- Strength
- 90 mg
- Approval
- NDA NDA022433
- On the market since
- Aug 5, 2011
- Package NDCs
55154-9618-055154-9618-8- Official label
- DailyMed (National Library of Medicine), updated Apr 14, 2026
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