NDC 10544-267
Levothyroxine Sodium 0.2 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged from NDC 0527-1351, 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 Blenheim Pharmacal, Inc. names for other drugs.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet
- Strength
- 0.2 mg
- Approval
- NDA NDA021210
- On the market since
- Nov 18, 2013
- Package NDCs
10544-267-30- Official label
- DailyMed (National Library of Medicine), updated Dec 22, 2015
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