Class III · Low risk
Mefenamic Acid
Failed Dissolution Specifications: Low dissolution results were obtained during stability testing
National Drug Code
Is NDC 66993-0070-30 recalled?
Mefenamic Acid
Yes — this exact package was recalled
2 FDA recalls name the code 66993-0070-30 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
Mefenamic Acid Capsules
Presence of foreign substance: The recall was initiated due to black particles being observed while performing routine post-release stability testing on Mefenamic acid capsules
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
- 66993-0019 Albuterol Sulfate HFA 1
- 66993-0408 See recall 1
- 66993-0463 See recall 1
- 66993-0473 Nisoldipine 1
- 66993-0485 See recall 1
- 66993-0680 See recall 1
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