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

Is NDC 63629-9204-01 recalled?

Cephalexin · 100 mL in 1 BOTTLE (63629-9204-1)

Yes — this exact package was recalled

1 FDA recall names the code 63629-9204-01 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
Cephalexin
Strength
CEPHALEXIN 125 mg/5mL
Form
For Suspension · Oral
Labeler
Bryant Ranch Prepack
Type
Human Prescription Drug
Product code
63629-9204

Recalls naming this package

Class III ยท Low risk

Cephalexin for Oral Suspension

Labeling: Not Elsewhere Classified: Front label states 100 Tablets instead of 100 ml and on the back label 'Each Tablet contains' instead of 'Each Bottle contains' No total dose per bottle listed should be 2.5 g'

Ongoing Labeling / mix-up Bryant Ranch Prepack, Inc. NDC 63629-9204-1 D-0536-2024

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