Class III · Low risk
Methylprednisolone Tablets
Subpotent
National Drug Code
Is NDC 59746-0001-06 recalled?
Methylprednisolone Tablets
Yes — this exact package was recalled
1 FDA recall names the code 59746-0001-06 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.
1 of these recalls is still ongoing.
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
Distributed by: DocRx
Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.
Class III · Low risk
Methylprednisolone Tablets USP
Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.
Class III · Low risk
MethylPREDNISolone Tablets
Failed Stability Specifications: An out-of-specification result was obtained during 18-month stability testing for assay.
Class II · Moderate risk
methylPREDNISolone Tablet
Labeling:Label Mixup; methylPREDNISolone Tablet, 4 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 137 mcg, NDC 00781519192, Pedigree: AD22616_10, EXP: 5/2/2014.
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
- 59746-0284 Pantoprazole Sodium 5
- 59746-0122 Meclizine Hydrochloride 2
- 59746-0360 valsartan 2
- 59746-0363 See recall 2
- 59746-0003 See recall 1
- 59746-0113 Prochlorperazine Maleate 1
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