Class II · Moderate risk
Aminophylline Injection
Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.
National Drug Code
Is NDC 0409-5921-01 recalled?
Aminophylline · 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-5921-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-5921-16)
Yes — this exact package was recalled
1 FDA recall names the code 0409-5921-01 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
- Aminophylline
- Strength
- AMINOPHYLLINE DIHYDRATE 25 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-5921
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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