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
- Dec 21, 2023 · Class I · Pfizer Inc.
Presence of Particulate Matter; identified as glass
Lots: Lot GY2496, Exp 02/01/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- NDA NDA021146
- On the market since
- Jan 19, 2006
- Package NDCs
0409-1630-100409-1630-15- Official label
- DailyMed (National Library of Medicine), updated May 18, 2026
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