Where it's made
This label doesn't name the factory that makes the drug. 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 IBSA Pharma Inc. names for other drugs.
Recalls
- Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220409, Exp. 10/2023; 220956, Exp. 03/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220413, Exp. 10/2023; 220964, Exp. 3/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220855, Exp. 2/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220416, Exp. 10/2023; 221053, Exp. 4/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220856, Exp. 2/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220552, Exp. 11/2023; 221055, Exp. 04/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220553, Exp. 11/2023; 221056, Exp. 04/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220407, Exp. 10/2023; 220960, Exp. 03/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220556, Exp. 11/2023; 221058, Exp. 04/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220853, Exp. 02/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220411, Exp. 10/2023; 220854, Exp. 02/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220414, Exp. 10/2023; 220852, Exp. 02/2024; 220970, Exp. 03/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220415, Exp. 10/2023; 221052, Exp. 04/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220959, Exp. 3/2024. - Jan 30, 2023 · Class II · Ibsa Pharma Inc
Subpotent Drug
Lots: Lot #: 220418, Exp. 10/2023; 220560, Exp. 11/2023.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- solution, oral
- Strength
- 25 ug per 1 mL
- Approval
- NDA NDA206977
- On the market since
- Mar 1, 2019
- Package NDCs
71858-0110-171858-0110-271858-0110-471858-0110-571858-0110-6- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?