NDC 68788-9160

Levothyroxine Sodium 0.025 mg tablet

On the label: Preferred Pharmaceuticals, Inc... It's repackaged from NDC 0527-1341, 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 Preferred Pharmaceuticals, Inc.. names for other drugs.

Product details

Generic drug
Levothyroxine: every company that makes it
Form
tablet
Strength
0.025 mg
Approval
NDA NDA021210
On the market since
Sep 9, 2009
Package NDCs
68788-9160-3 68788-9160-9
Official label
DailyMed (National Library of Medicine), updated Feb 1, 2017

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