NDC 82804-085
Eliquis 5 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from E.R. Squibb & Sons, L.L.C.'s NDC 0003-0894.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that packages it and labels it). 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 E.R. Squibb & Sons, L.L.C. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Jun 5, 2017 · Class I · Bristol-myers Squibb Company
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
Lots: Lot: HN0063, EXP. 09/2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Apixaban: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- NDA NDA202155
- On the market since
- Dec 28, 2012
- Package NDCs
82804-085-3082804-085-31- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?