Class II · Moderate risk
Mercaptopurine Tablets
Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
National Drug Code
Is NDC 49884-0922-02 recalled?
Mercaptopurine Tablets
Yes — this exact package was recalled
2 FDA recalls name the code 49884-0922-02 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls naming this package
Class II · Moderate risk
Mercaptopurine Tablets
Failed USP Dissolution Test Requirements: The recalled lots do not meet the specification for dissolution.
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
- 49884-0125 See recall 2
- 49884-0306 Clonazepam 2
- 49884-0034 See recall 1
- 49884-0035 See recall 1
- 49884-0038 See recall 1
- 49884-0065 Glycopyrrolate 1
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