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

Is NDC 0338-0108-20 recalled?

Norepinephrine Bitartrate · 20 CONTAINER in 1 CARTON (0338-0108-20) / 250 mL in 1 CONTAINER

Yes — this exact package was recalled

1 FDA recall names the code 0338-0108-20 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.

1 of these recalls is still ongoing.

Active ingredient
norepinephrine bitartrate
Strength
NOREPINEPHRINE BITARTRATE 8 mg/250mL
Form
Injection, Solution · Intravenous
Labeler
Baxter Healthcare Corporation
Type
Human Prescription Drug
Product code
0338-0108

Recalls naming this package

Class II · Moderate risk

Norepinephrine Bitartrate in 5% Dextrose Injection

Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL.

Ongoing Labeling / mix-up Baxter Healthcare Corporation D-0336-2024

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