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

Is NDC 0487-5901-99 recalled?

S2 · 30 POUCH in 1 CARTON (0487-5901-99) / 1 VIAL, SINGLE-USE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-USE

Yes — this exact package was recalled

2 FDA recalls name the code 0487-5901-99 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
racepinephrine hydrochloride
Strength
RACEPINEPHRINE HYDROCHLORIDE 11.25 mg/.5mL
Form
Solution · Respiratory (inhalation)
Labeler
Nephron Pharmaceuticals Corporation
Type
Human OTC Drug
Product code
0487-5901

Recalls naming this package

Class II · Moderate risk

Racepinephrine Inhalation Solution

CGMP Deviations: products were stored outside the drug label specifications.

Terminated Labeling / mix-up Mckesson Medical-Surgical Inc. Corporate Office NDC 0487-5901-99 D-1325-2022

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