NDC 71205-232
Levothyroxine sodium 125 ug tablet
On the label: Proficient Rx LP. It's repackaged from NDC 0781-5186, made by Sandoz 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 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 Proficient Rx LP names for other drugs.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet
- Strength
- 125 ug
- Approval
- NDA authorized generic NDA021342
- On the market since
- Mar 1, 2002
- Package NDCs
71205-232-3071205-232-6071205-232-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?