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

Is NDC 0378-9651-32 recalled?

Travoprost Ophthalmic Solution, 0.004% · 1 BOTTLE in 1 CARTON (0378-9651-32) / 2.5 mL in 1 BOTTLE

Yes — this exact package was recalled

1 FDA recall names the code 0378-9651-32 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
Travoprost Ophthalmic Solution, 0.004%
Strength
TRAVOPROST .04 mg/mL
Form
Solution/ Drops · Ophthalmic
Labeler
Mylan Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
0378-9651

Recalls naming this package

Class II ยท Moderate risk

Travoprost Ophthalmic Solution

Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance impurities/degradation during routine stability testing.

Terminated Impurity / degradation Mylan Pharmaceuticals Inc NDC 0378-9651-32 D-0748-2022

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