Class II · Moderate risk
Estradiol 25mg pellet
Lack of Assurance of Sterility
National Drug Code
Is NDC 69761-0025-12 recalled?
Estradiol 25mg pellet
Yes — this exact package was recalled
1 FDA recall names the code 69761-0025-12 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
Estradiol 25 mg pellet 99.5% Estradiol USP
CGMP deviations- Lack of Quality Assurance
Class II · Moderate risk
Estradiol USP 99.5%
Lack of Assurance of Sterility: The firm is recalling all sterile preparations within expiry due to deficient practices which may have an impact on sterility assurance.
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
- 69761-0006 See recall 3
- 69761-0010 See recall 3
- 69761-0012 See recall 3
- 69761-0015 See recall 3
- 69761-0018 See recall 3
- 69761-0020 See recall 3
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