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

Is NDC 0004-0260-01 recalled?

CellCept · 1 BOTTLE, PLASTIC in 1 CARTON (0004-0260-01) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Yes — this exact package was recalled

1 FDA recall names the code 0004-0260-01 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.

Active ingredient
Mycophenolate Mofetil
Strength
MYCOPHENOLATE MOFETIL 500 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Genentech, Inc.
Type
Human Prescription Drug
Product code
0004-0260

Recalls naming this package

Class II ยท Moderate risk

Mycophenolate Mofetil

Labeling: Label Mixup: MYCOPHENOLATE MOFETIL, Tablet, 500 mg may be potentially mis-labeled as the following drug: MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 00004025901, Pedigree: AD49414_1, EXP: 5/17/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-772-2014

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