NDC 70594-095
Ceftriaxone 500 mg injection, powder, for solution
On the label: Xellia Pharmaceuticals USA LLC.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Xellia Pharmaceuticals USA LLC names for other drugs.
Recalls
- May 15, 2023 · Class II · Astral SteriTech Private Ltd.
Lack of Assurance of Sterility
Lots: All lots within expiry.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ceftriaxone: every company that makes it
- Form
- injection, powder, for solution
- Strength
- 500 mg
- Approval
- ANDA ANDA091049
- On the market since
- Jan 6, 2022
- Package NDCs
70594-095-0170594-095-02- Official label
- DailyMed (National Library of Medicine), updated Apr 7, 2022
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