NDC 54458-890
Montelukast 10 mg tablet, film coated
On the label: International Laboratories, LLC. It's repackaged from NDC 0093-7426, made by Teva Pharmaceuticals USA, Inc. (Montelukast Sodium). 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 (it lists 1 site that repackages it and relabels 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 International Laboratories, LLC names for other drugs.
Product details
- Generic drug
- Montelukast: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA078605
- On the market since
- Oct 4, 2013
- Package NDCs
54458-890-10- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2017
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