Class III · Low risk
Asmanex Twisthaler
Defective Container
National Drug Code
Is NDC 78206-0114-04 recalled?
Asmanex · 1 POUCH in 1 CARTON (78206-114-04) / 1 INHALER in 1 POUCH / 30 INHALANT in 1 INHALER
Yes — this exact package was recalled
1 FDA recall names the code 78206-0114-04 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.
3 of these recalls are still ongoing.
- Active ingredient
- Mometasone Furoate
- Strength
- MOMETASONE FUROATE 220 ug/1
- Form
- Inhalant · Respiratory (inhalation)
- Labeler
- Organon LLC
- Type
- Human Prescription Drug
- Product code
- 78206-0114
Recalls naming this package
Class III · Low risk
Asmanex Twisthaler
Defective Container
Class III · Low risk
Asmanex Twisthaler
Defective Container
Class II · Moderate risk
Asmanex Twisthaler
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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
- 78206-0183 Hadlima 1
Free recall alerts
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