NDC 53808-0846
Levothyroxine Sodium 0.112 mg tablet
On the label: State of Florida DOH Central Pharmacy. 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 State of Florida DOH Central Pharmacy 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
- Jan 1, 2013
- Package NDCs
53808-0846-1- Official label
- DailyMed (National Library of Medicine), updated Sep 13, 2013
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