NDC 50436-5501
Levothyroxine Sodium 0.112 mg tablet
On the label: Unit Dose Services. It's repackaged from NDC 0527-1346, made by Lannett Company, Inc. (Levothyroxine 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). 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 Unit Dose Services names for other drugs.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet
- Strength
- 0.112 mg
- Approval
- NDA NDA021210
- On the market since
- Dec 1, 2003
- Package NDCs
50436-5501-250436-5501-3- Official label
- DailyMed (National Library of Medicine), updated Mar 7, 2012
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