Class II · Moderate risk
Inhub Wixela
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
National Drug Code
Is NDC 0378-9320-32 recalled?
Wixela Inhub · 1 INHALER in 1 CARTON (0378-9320-32) / 60 POWDER in 1 INHALER
Yes — this exact package was recalled
1 FDA recall names the code 0378-9320-32 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
- fluticasone propionate and salmeterol
- Strength
- FLUTICASONE PROPIONATE 100 ug/1; SALMETEROL XINAFOATE 50…
- Form
- Powder · Respiratory (inhalation)
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 0378-9320
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
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.