Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 71858-0145-05 recalled?

Tirosint SOL · 6 POUCH in 1 CARTON (71858-0145-5) / 5 AMPULE in 1 POUCH (71858-0145-4) / 1 mL in 1 AMPULE (71858-0145-6)

Yes — this exact package was recalled

1 FDA recall names the code 71858-0145-05 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Levothyroxine Sodium
Strength
LEVOTHYROXINE SODIUM 137 ug/mL
Form
Solution · Oral
Labeler
IBSA Pharma Inc.
Type
Human Prescription Drug
Product code
71858-0145

Recalls naming this package

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler