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

Is NDC 49884-0161-11 recalled?

Calcitonin Salmon · 3.7 mL in 1 BOTTLE, GLASS (49884-161-11)

Yes — this exact package was recalled

1 FDA recall names the code 49884-0161-11 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
Calcitonin Salmon
Strength
CALCITONIN SALMON 200 [iU]/.09mL
Form
Spray, Metered · Nasal
Labeler
Par Health USA, LLC
Type
Human Prescription Drug
Product code
49884-0161

Recalls naming this package

Class II · Moderate risk

Calcitonin Salmon Nasal Spray

Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of Specification results for a known and unknown impurity as well as low Out of Specification results for assay.

Terminated Impurity / degradation Endo Pharmaceuticals, Inc. NDC 49884-161-11 D-0475-2023

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