Class II ยท Moderate risk
Azacitidine for Injection 100mg/Vial
Lack of Sterility Assurance
National Drug Code
Is NDC 70069-0857-01 recalled?
Azacitidine · 1 VIAL, GLASS in 1 CARTON (70069-857-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 70069-0857-01 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
- Azacitidine
- Strength
- AZACITIDINE 100 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous, Subcutaneous
- Labeler
- Somerset Therapeutics LLC
- Type
- Human Prescription Drug
- Product code
- 70069-0857
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
- 70069-0381 Haloperidol Decanoate 2
- 70069-0025 Dexamethasone Sodium Phosphate 1
- 70069-0101 Methocarbamol 1
- 70069-0141 Cisatracurium Besylate 1
- 70069-0151 Cisatracurium Besylate 1
- 70069-0161 Cisatracurium Besylate 1
Free recall alerts
Know the day your medication is recalled
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