NDC 0409-7338
Ceftriaxone Sodium 500 mg injection, powder, for solution
On the label: Hospira, Inc..
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 Hospira, Inc. names for other drugs.
Recalls
- Oct 19, 2016 · Class III · Sandoz Inc
Labeling: Missing Label
Lots: Sandoz - Lot GJ7151(Pfizer- Lot 670028M); Exp. 07/19
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, intramuscular; intravenous
- Strength
- 500 mg
- Approval
- ANDA ANDA065169
- On the market since
- May 9, 2005
- Package NDCs
0409-7338-010409-7338-11- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?