NDC 54868-5986
Trilipix 135 mg capsule, delayed release
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0074-9189, made by AbbVie Inc. (Trilipix). That product's FDA listing has since ended, so its label and factories are no longer published.
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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, delayed release
- Strength
- 135 mg
- Approval
- NDA NDA022224
- On the market since
- Feb 19, 2009
- Package NDCs
54868-5986-054868-5986-1- Official label
- DailyMed (National Library of Medicine), updated Dec 14, 2011
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