Class III ยท Low risk
Zithromax (azithromycin for injection)
Failed Impurities/Degradation Specifications: Pfizer is recalling certain lots due to out of specification results for azithromycin N-oxide degradant.
National Drug Code
Is NDC 0069-3150-84 recalled?
Zithromax
Yes — this exact package was recalled
1 FDA recall names the code 0069-3150-84 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
- azithromycin dihydrate
- Strength
- AZITHROMYCIN DIHYDRATE 500 mg/5mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 0069-3150
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
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