Class II · Moderate risk
Kit for the Preparation of Technetium TC-99M Mebrofenin
Failed Stability Specifications
National Drug Code
Is NDC 45567-0455-01 recalled?
Kit for the Preparation of Technetium Tc 99m Mebrofenin · 5 VIAL, MULTI-DOSE in 1 KIT (45567-0455-1) / 10 mL in 1 VIAL, MULTI-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 45567-0455-01 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.
- Active ingredient
- Kit for the Preparation of Technetium Tc 99m Mebrofenin
- Strength
- MEBROFENIN 45 mg/10mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 45567-0455
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
- 45567-0040 Kit for the Preparation of Technetium Tc 99M Medronate 1
- 45567-0555 See recall 1
- 45567-0655 Kit for the Preparation of Technetium Tc99m Mertiatide 1
Free recall alerts
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