Class II · Moderate risk
traMADol HCl Tablet
Labeling:Label Mixup; traMADol HCl Tablet, 25 mg (1/2 of 50 mg) may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 137 mcg, NDC 00527163801, Pedigree: AD60272_76, EXP: 5/22/2014.
National Drug Code
Is NDC 57664-0377-18 recalled?
traMADol HCl Tablet
Yes — this exact package was recalled
1 FDA recall names the code 57664-0377-18 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
traMADOL Hydrochloride Tablets
Adulterated Presence of Foreign Tablets: A customer complaint was received that a bottle of Tramadol HCl Tablets USP 50 mg contained some tablets of Metoprolol Tartrate Tablets USP, 50 mg.
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
- 57664-0051 Lisdexamfetamine Dimesylate 2
- 57664-0135 See recall 2
- 57664-0506 See recall 2
- 57664-0783 See recall 2
- 57664-0046 Lisdexamfetamine Dimesylate 1
- 57664-0047 Lisdexamfetamine Dimesylate 1
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