NDC 23155-216
Cidofovir Dihydrate 375 mg per 5 mL injection, solution
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Maiva Pharma Private Limited | Hosur, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 29, 2022 · 1 inspection |
Recalls
- Oct 15, 2018 · Class II · Heritage Pharmaceuticals, Inc.
Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
Lots: Lot #: VCIA083, Exp. JUN2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cidofovir: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 375 mg per 5 mL
- Approval
- ANDA ANDA202501
- On the market since
- Aug 6, 2012
- Package NDCs
23155-216-31- Official label
- DailyMed (National Library of Medicine), updated Oct 25, 2023
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