Class I · High risk
Amikacin Sulfate Injection
Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) .
National Drug Code
Is NDC 23155-0290-32 recalled?
Amikacin Sulfate
Yes — this exact package was recalled
1 FDA recall names the code 23155-0290-32 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
- Amikacin Sulfate
- Strength
- AMIKACIN SULFATE 250 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 23155-0290
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
- 23155-0110 See recall 3
- 23155-0645 See recall 3
- 23155-0646 See recall 3
- 23155-0216 Cidofovir Dihydrate 2
- 23155-0490 Desmopressin Acetate 2
- 23155-0002 See recall 1
Free recall alerts
Know the day your medication is recalled
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