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

Is NDC 55150-0330-01 recalled?

Medroxyprogesterone Acetate · 1 SYRINGE in 1 CARTON (55150-330-01) / 1 mL in 1 SYRINGE

Yes — this exact package was recalled

1 FDA recall names the code 55150-0330-01 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
Medroxyprogesterone Acetate
Strength
MEDROXYPROGESTERONE ACETATE 150 mg/mL
Form
Injection, Suspension · Intramuscular
Labeler
Eugia US LLC
Type
Human Prescription Drug
Product code
55150-0330

Recalls naming this package

Class II · Moderate risk

Medroxyprogesterone Acetate Injectable Suspension

Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.

Ongoing Temperature excursion Mckesson Medical-Surgical Inc. Corporate Office NDC 55150-0330-01 D-0400-2025

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