Class III · Low risk
Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution 3mL vial
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0487-0201-60 recalled?
Ipratropium Bromide and Albuterol Sulfate · 12 POUCH in 1 CARTON (0487-0201-60) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE
Yes — this exact package was recalled
2 FDA recalls name the code 0487-0201-60 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 Sulfate
- Strength
- IPRATROPIUM BROMIDE .5 mg/3mL; ALBUTEROL SULFATE 3 mg/3mL
- Form
- Solution · Respiratory (inhalation)
- Labeler
- Nephron Pharmaceuticals Corporation
- Type
- Human Prescription Drug
- Product code
- 0487-0201
Recalls naming this package
Class II · Moderate risk
Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution
Lack of Assurance of Sterility; potential exposure to non-sterile lubricant during the filling process
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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