NDC 84549-820
DOPamine Hydrochloride 40 mg per 1 mL injection, solution, concentrate
On the label: ProPharma Distribution. It's repackaged: ProPharma Distribution rebottles it from Hospira, Inc.'s NDC 0409-5820.
Where the pills inside were 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 |
Repackaging site
- ProPharma Distribution, Westminster, CO, United States · repackages it and relabels it
Recalls
- Sep 4, 2026 · Class II · Pfizer
Lack of Assurance of Sterility
Lots: Lot # NL5230, Exp Date:10/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dopamine: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 40 mg per 1 mL
- Approval
- NDA NDA018132
- On the market since
- Aug 25, 2005
- Package NDCs
84549-820-01- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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