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

Is NDC 55111-0163-30 recalled?

Olanzapine · 30 TABLET, FILM COATED in 1 BOTTLE (55111-163-30)

Yes — this exact package was recalled

1 FDA recall names the code 55111-0163-30 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
Olanzapine
Strength
OLANZAPINE 2.5 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Dr. Reddy's Laboratories Ltd.
Type
Human Prescription Drug
Product code
55111-0163

Recalls naming this package

Class III ยท Low risk

Olanzapine tablets

Failed impurities/degradation specifications: due to out-of-specification result for the Related Substance Compound C (Impurity 6 - N-Oxide at the 18 month stability station.

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-163-30 D-0468-2017

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