Class III · Low risk
Valsartan Tablets USP
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
National Drug Code
Is NDC 59746-0363-90 recalled?
Valsartan Tablets USP
Yes — this exact package was recalled
2 FDA recalls name the code 59746-0363-90 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 III · Low risk
Valsartan Tablets USP
Incorrect/Undeclared excipient: Product batches were released into commercial distribution with a larger size grade of excipient (Crospovidone).
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
- 59746-0001 See recall 5
- 59746-0284 Pantoprazole Sodium 5
- 59746-0122 Meclizine Hydrochloride 2
- 59746-0360 valsartan 2
- 59746-0003 See recall 1
- 59746-0113 Prochlorperazine Maleate 1
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