Class III · Low risk
MethylPREDNISolone TABLETS
Subpotent; 6 month stability time point
National Drug Code
Is NDC 0603-4593-21 recalled?
MethylPREDNISolone · 100 TABLET in 1 BOTTLE, PLASTIC (0603-4593-21)
Yes — this exact package was recalled
2 FDA recalls name the code 0603-4593-21 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.
- Active ingredient
- methylprednisolone
- Strength
- METHYLPREDNISOLONE 4 mg/1
- Form
- Tablet · Oral
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug
- Product code
- 0603-4593
Recalls naming this package
Class II · Moderate risk
methylPREDNISolone
Labeling: Label Mixup: methylPREDNISolone, Tablet, 4 mg may have potentially been mislabeled as the following drug: OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/110 mg, NDC 11523726503, Pedigree: AD42584_15, EXP: 5/14/2014.
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
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