Class II · Moderate risk
Budesonide and Formoterol Fumarate Dihydrate Inhalation Aerosol…
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 0310-7372-20 recalled?
Budesonide and Formoterol Fumarate Dihydrate · 1 POUCH in 1 CARTON (0310-7372-20) / 1 CANISTER in 1 POUCH / 120 AEROSOL in 1 CANISTER
Yes — this exact package was recalled
1 FDA recall names the code 0310-7372-20 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
- Budesonide and Formoterol Fumarate Dihydrate
- Strength
- BUDESONIDE 80 ug/1; FORMOTEROL FUMARATE 4.5 ug/1
- Form
- Aerosol · Respiratory (inhalation)
- Labeler
- AstraZeneca Pharmaceuticals LP
- Type
- Human Prescription Drug
- Product code
- 0310-7372
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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