Class II · Moderate risk
Kit for the Preparation of Technetium Tc 99m Mertiatide
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
National Drug Code
Is NDC 45567-0655-01 recalled?
Kit for the Preparation of Technetium Tc99m Mertiatide · 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1)
Yes — this exact package was recalled
1 FDA recall names the code 45567-0655-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Betiatide
- Strength
- BETIATIDE 1 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 45567-0655
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
- 45567-0455 Kit for the Preparation of Technetium Tc 99m Mebrofenin 1
- 45567-0555 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.