Class II · Moderate risk
Betamethasone Dipropionate Lotion USP
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
National Drug Code
Is NDC 52565-0023-59 recalled?
Betamethasone Dipropionate Lotion USP
Yes — this exact package was recalled
1 FDA recall names the code 52565-0023-59 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
Betamethasone Dipropionate Lotion USP
Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
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
- 52565-0008 See recall 3
- 52565-0009 See recall 3
- 52565-0019 See recall 3
- 52565-0002 See recall 2
- 52565-0010 See recall 2
- 52565-0014 See recall 2
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