Class II · Moderate risk
dilTIAZem 125mg/125mL
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
National Drug Code
Is NDC 72196-6054-01 recalled?
dilTIAZem 125mg/125mL
Yes — this exact package was recalled
2 FDA recalls name the code 72196-6054-01 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
dilTIAZem 125mg/125mL
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
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
- 72196-0100 See recall 2
- 72196-0103 See recall 2
- 72196-0105 See recall 2
- 72196-0111 See recall 2
- 72196-0202 See recall 2
- 72196-0211 See recall 2
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