Class II · Moderate risk
Solifenacin Succinate Tablets
CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might convert to Solifenacin Tartrate Tablets.
National Drug Code
Is NDC 51991-0894-33 recalled?
Solifenacin Succinate Tablets
Yes — this exact package was recalled
1 FDA recall names the code 51991-0894-33 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
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
- 51991-0748 Duloxetine Delayed-Release 11
- 51991-0747 Duloxetine Delayed-Release 6
- 51991-0746 Duloxetine Delayed-Release 3
- 51991-0014 See recall 1
- 51991-0064 See recall 1
- 51991-0457 See recall 1
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