Class II · Moderate risk
Cidofovir Injection 375mg/5mL
Lack of Assurance of Sterility: complaints received about dried powder on the outside of bottle
National Drug Code
Is NDC 23155-0216-31 recalled?
Cidofovir Dihydrate · 5 mL in 1 VIAL, GLASS (23155-216-31)
Yes — this exact package was recalled
2 FDA recalls name the code 23155-0216-31 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
- Cidofovir Dihydrate
- Strength
- CIDOFOVIR 375 mg/5mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 23155-0216
Recalls naming this package
Class II · Moderate risk
Cidofovir injection 375 mg/mL
Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
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
- 23155-0490 Desmopressin Acetate 2
- 23155-0002 See recall 1
- 23155-0004 See recall 1
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