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

Is NDC 69918-0301-30 recalled?

Tranexamic Acid · 30 TABLET in 1 BOTTLE (69918-301-30)

Yes — this exact package was recalled

1 FDA recall names the code 69918-0301-30 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
Tranexamic Acid
Strength
TRANEXAMIC ACID 650 mg/1
Form
Tablet · Oral
Labeler
Nordic Pharma, Inc.
Type
Human Prescription Drug
Product code
69918-0301

Recalls naming this package

Class III · Low risk

Lysteda (tranexamic acid)

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation Amring Pharmaceuticals Inc NDC 69918-301-30 D-0871-2023

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