Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213 India. Manufactured for BluePoint Laboratories. NDC 68001-0313-56
Reported: August 24, 2022 Initiated: July 27, 2022 #D-1349-2022
Product Description
Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213 India. Manufactured for BluePoint Laboratories. NDC 68001-0313-56
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Amerisource Health Services LLC
- Units Affected
- 4,160 vials
- Distribution
- Nationwide within the USA
- Location
- Columbus, OH
Frequently Asked Questions
What product was recalled? ▼
Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213 India. Manufactured for BluePoint Laboratories. NDC 68001-0313-56. Recalled by Amerisource Health Services LLC. Units affected: 4,160 vials.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 24, 2022. Severity: Low. Recall number: D-1349-2022.
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