NDC 0074-9296

Synthroid 112 ug tablet

On the label: AbbVie Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants AbbVie Inc. uses for other drugs.

Recalls

• Oct 17, 2023 · Class III · Ongoing
  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 · Terminated
  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 · Terminated
  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 · Terminated
  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 · Terminated
  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

Product details

Generic drug

Levothyroxine: see every company that makes it

Form

tablet, oral

Strength

112 ug

Approval

NDA NDA021402

On the market since

Jul 24, 2002

Package NDCs

0074-9296-13 0074-9296-19 0074-9296-71 0074-9296-72 0074-9296-90

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?