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

Is NDC 29300-0415-19 recalled?

Cyclobenzaprine hydrochloride · 90 TABLET, FILM COATED in 1 BOTTLE (29300-415-19)

Yes — this exact package was recalled

1 FDA recall names the code 29300-0415-19 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
Cyclobenzaprine hydrochloride
Strength
CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Unichem Pharmaceuticals (USA), Inc.
Type
Human Prescription Drug
Product code
29300-0415

Recalls naming this package

Class I · High risk

Cyclobenzaprine Hydrochloride Tablets

Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).

Ongoing Labeling / mix-up Unichem Pharmaceuticals USA Inc. NDC 29300-415-19 D-0655-2025

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