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 |
| Hospira, Inc. | Location not on file | Tests it | Not inspected on record |
Recalls
- Dec 21, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter; identified as glass
Lots: Lot GX1542, Exp. 01/01/2025 - Oct 2, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter: identified as glass.
Lots: Lot#: GJ5007, Exp. 8/1/2024
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
- Strength
- 42 mg per 1 mL
- Approval
- ANDA ANDA202679
- On the market since
- Aug 17, 2020
- Package NDCs
0409-5534-140409-5534-24- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?