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

Is NDC 42192-0501-05 recalled?

Doxycycline · 500 TABLET, COATED in 1 BOTTLE (42192-501-05)

Yes — this exact package was recalled

1 FDA recall names the code 42192-0501-05 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
Doxycycline hyclate
Strength
DOXYCYCLINE HYCLATE 100 mg/1
Form
Tablet, Coated · Oral
Labeler
Acella Pharmaceuticals, LLC
Type
Human Prescription Drug
Product code
42192-0501

Recalls naming this package

Class II ยท Moderate risk

Doxycycline Hyclate Tablets

Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.

Ongoing Dissolution failure Acella Pharmaceuticals, LLC NDC 42192-501-05 D-0014-2026

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