Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01, For Intravenous Infusion Only MUST BE DILUTED PRIOR TO USE, packaged in 10 x 20mL Single-Dose Vials per pack NDC 68382-049-10, Rx only, Manufactured by: Cadila Healthcare Ltd., Vadodara, India. Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534.
Drug Recall
Official source record
- Recall number
- D-0315-2021
- Event ID
- 87364
- Classification
- Class I
- Status
- Terminated
- Recalling company
- Zydus Pharmaceuticals (USA) Inc
- Reason for recall
- Crystallization: customer complaints for crystallization in finished product.
- Report date
- April 7, 2021
- Recall initiation date
- February 18, 2021
- Termination date
- November 23, 2022
- Distribution pattern
- USA Nationwide
Drug product identifiers
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc.
- Brand name
- ACYCLOVIR
- Generic name
- ACYCLOVIR
- Substance name
- ACYCLOVIR SODIUM
- Product NDCs
- 68382-048; 68382-049
- Package NDCs
- 68382-048-01; 68382-048-10; 68382-049-01; 68382-049-10
- Route
- INTRAVENOUS
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.
Where can I find more official information?
The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.
