Class II ยท Moderate risk
Azacitidine for Injection 100 mg/vial
CGMP Deviations
National Drug Code
Is NDC 72485-0201-01 recalled?
Azacitidine · 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (72485-201-01)
Yes — this exact package was recalled
1 FDA recall names the code 72485-0201-01 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
- azacitidine
- Strength
- AZACITIDINE 100 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous, Subcutaneous
- Labeler
- Armas Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 72485-0201
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
- 72485-0202 Imatinib mesylate 1
- 72485-0203 Imatinib mesylate 400 mg 1
- 72485-0210 See recall 1
- 72485-0216 See recall 1
- 72485-0221 See recall 1
- 72485-0502 Milrinone Lactate 1
Free recall alerts
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