Class II ยท Moderate risk
Aminaocaproic Acid Injection
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
National Drug Code
Is NDC 0517-9120-01 recalled?
Aminocaproic Acid
Yes — this exact package was recalled
1 FDA recall names the code 0517-9120-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Aminocaproic Acid
- Strength
- AMINOCAPROIC ACID 250 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- American Regent, Inc.
- Type
- Human Prescription Drug
- Product code
- 0517-9120
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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