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 AbbVie Inc. names for other drugs.
Recalls
- Oct 17, 2023 · Class III · AbbVie Inc.
Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.
Lots: Lot # 1187435 exp date: 02/2024 - Dec 4, 2012 · Class II · Abbott Laboratories
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Lots: LOT # 18262A8 Exp. 09/13 - Jul 19, 2012 · Class II · Abbott Laboratories
Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
Lots: 18265A8, Exp 09/20/2013 - Jul 19, 2012 · Class II · Abbott Laboratories
Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
Lots: Lot: 18353A8, Exp 08/31/2013 - Jul 19, 2012 · Class II · Abbott Laboratories
Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
Lots: Lot: 18355A8, Exp. 09/26/13
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
- tablet, oral
- Strength
- 200 ug
- Approval
- NDA NDA021402
- On the market since
- Feb 24, 2002
- Package NDCs
0074-7148-110074-7148-190074-7148-710074-7148-720074-7148-90- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?