Class II · Moderate risk
Combivent Respimat
Defective Delivery System: Inhalers do not spray properly, emitting either no spray or a short transient spray.
National Drug Code
Is NDC 0597-0024-02 recalled?
Combivent Respimat · 1 CARTRIDGE in 1 CARTON (0597-0024-02) / 120 SPRAY, METERED in 1 CARTRIDGE
Yes — this exact package was recalled
1 FDA recall names the code 0597-0024-02 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
- ipratropium bromide and albuterol
- Strength
- IPRATROPIUM BROMIDE 20 ug/1; ALBUTEROL SULFATE 100 ug/1
- Form
- Spray, Metered · Respiratory (inhalation)
- Labeler
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 0597-0024
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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