Class III · Low risk
Anoro Ellipta
Failed Release Testing: Coarse Particle Mass for umeclidinium Out of Specification
National Drug Code
Is NDC 0173-0869-10 recalled?
Anoro Ellipta · 1 TRAY in 1 CARTON (0173-0869-10) / 1 INHALER in 1 TRAY / 30 POWDER in 1 INHALER
Yes — this exact package was recalled
1 FDA recall names the code 0173-0869-10 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
- umeclidinium bromide and vilanterol trifenatate
- Strength
- UMECLIDINIUM BROMIDE 62.5 ug/1; VILANTEROL TRIFENATATE 25…
- Form
- Powder · Respiratory (inhalation)
- Labeler
- GlaxoSmithKline LLC
- Type
- Human Prescription Drug
- Product code
- 0173-0869
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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