Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
Recalls
- Aug 4, 2025 · Class II · Pfizer Inc
Lack of Assurance of Sterility.
Lots: Lot #: LH2671, Exp. 11/30/2026 - Dec 21, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter; identified as glass
Lots: Lot HA7295, EXP 03/01/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 84 mg per 1 mL
- Approval
- ANDA ANDA202494
- On the market since
- Jul 23, 2020
- Package NDCs
0409-6637-140409-6637-24- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?