Class II ยท Moderate risk
Taztia XT
Failed Dissolution Specification: Out of a specification result occurred during the 3-month stability testing. Dissolution result at the 4-hour time point was 41% (specification: 20-40%).
National Drug Code
Is NDC 62037-0700-90 recalled?
Taztia XT
Yes — this exact package was recalled
1 FDA recall names the code 62037-0700-90 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
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
- 62037-0571 See recall 1
- 62037-0577 See recall 1
- 62037-0597 Cartia XT 1
- 62037-0600 Cartia XT 1
- 62037-0696 See recall 1
- 62037-0725 Methylphenidate Hydrochloride 1
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