Class III · Low risk
Advair HFA
Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.
National Drug Code
Is NDC 0173-0715-22 recalled?
Advair Hfa · 1 INHALER in 1 CARTON (0173-0715-22) / 60 AEROSOL, METERED in 1 INHALER
Yes — this exact package was recalled
1 FDA recall names the code 0173-0715-22 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 xinafoate
- Strength
- FLUTICASONE PROPIONATE 45 ug/1; SALMETEROL XINAFOATE 21 ug/1
- Form
- Aerosol, Metered · Respiratory (inhalation)
- Labeler
- GlaxoSmithKline LLC
- Type
- Human Prescription Drug
- Product code
- 0173-0715
Recalls naming this package
Class III · Low risk
Advair HFA
Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.
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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