NDC 68084-879
Cyclosporine 25 mg capsule, gelatin coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Apotex Corp.'s NDC 60505-0133.
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 Apotex Corp. names for other drugs.
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Feb 8, 2017 · Class II · Amerisource Health Services
Failed Impurities/Degradations Specifications; out of specification results for Maximum Unknown Impurities and Total Impurities
Lots: Lot 154527, exp 4/30/2017 - Feb 3, 2017 · Class II · Apotex Inc.
Failed Impurities/Degradations Specifications; out of specification results for Maximum Unknown Impurities and Total Impurities.
Lots: Lot MJ9837, Exp 07/2017. NDC 60505-0134-0, UPC 360505013401
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cyclosporine: every company that makes it
- Form
- capsule, gelatin coated, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA065040
- On the market since
- Sep 30, 2015
- Package NDCs
68084-879-2568084-879-95- Official label
- DailyMed (National Library of Medicine), updated May 13, 2024
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