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

Is NDC 42023-0116-02 recalled?

Pitocin · 25 VIAL in 1 CARTON (42023-116-02) / 10 mL in 1 VIAL

Yes — this exact package was recalled

1 FDA recall names the code 42023-0116-02 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
oxytocin
Strength
OXYTOCIN 10 [iU]/mL
Form
Injection · Intravenous
Labeler
Par Health USA, LLC
Type
Human Prescription Drug
Product code
42023-0116

Recalls naming this package

Class III · Low risk

Pitocin (Oxytocin Injection, USP)

Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store between 20¿ to 25¿C (68¿ to 77¿F)". Pitocin lot 225867 and part of Pitocin lot 231423 were labeled, "Store between 20¿ to 25¿C (28¿ to 77¿F)".

Terminated Labeling / mix-up JHP Pharmaceuticals, LLC NDC 42023-116-02 D-1420-2012

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