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 |
| Pfizer Healthcare India Private Limited | Anakapalli, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action |
Recalls
- May 3, 2021 · Class II · Pfizer Inc.
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Lots: Lot DN9185
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Water: every company that makes it
- Form
- injection, intramuscular; intravenous; subcutaneous
- Strength
- 1 mL per 1 mL
- Approval
- NDA NDA018801
- On the market since
- Jun 16, 2005
- Package NDCs
0409-4887-050409-4887-100409-4887-170409-4887-200409-4887-230409-4887-240409-4887-250409-4887-310409-4887-320409-4887-340409-4887-500409-4887-99- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?