NDC 0338-1007
Dopamine Hydrochloride and Dextrose 160 mg per 100 mL injection, solution
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Healthcare Corporation | Marion, NC, United States | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionFeb 9, 2024 · 9 inspections, 3 with FDA action |
| Baxter Healthcare Corporation | Jayuya, PR, United States | Makes it, tests it, packages it, labels it and sterilizes it | Problems found, fixed voluntarilyJul 19, 2024 · 15 inspections, 5 with FDA action |
| Baxter Healthcare Corporation | Round Lake, IL, United States | Tests it | Serious problems, FDA actionApr 2, 2026 · 15 inspections, 2 with FDA action |
Recalls
- Sep 29, 2014 · Class II · Baxter Healthcare Corp.
Lack of Assurance of Sterility: A small cut in the solution bag may have been introduced during the manufacturing process, resulting in a leak of the bag into the overpouch.
Lots: Lot# P303172; Exp. 12/14
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, intravenous
- Strength
- 160 mg per 100 mL
- Approval
- NDA NDA019615
- On the market since
- Mar 27, 1987
- Package NDCs
0338-1007-020338-1007-03- Official label
- DailyMed (National Library of Medicine), updated Nov 11, 2020
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