Quick answers
- What is Dopamine Hci?
- Dopamine Hci is a brand name of Dopamine hydrochloride, a prescription medicine. The FDA NDC Directory lists 2 Dopamine Hci products in 1 strength and form.
- Who makes Dopamine Hci?
- Hospira holds the FDA application for Dopamine Hci (NDA018132, approved May 19, 1981). 1 other company (repackagers or distributors) also list Dopamine Hci products.
- Is there a generic or store brand of Dopamine Hci?
- Yes. The FDA NDC Directory lists 6 other products with the same active ingredients, strength and form as a Dopamine Hci product. Ask your pharmacist whether one is right for you.
- Has Dopamine Hci been recalled?
- No recall linked to Dopamine Hci products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Dopamine Hci is
Each Dopamine Hci product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Dopamine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dopamine hydrochloride 40 mg/mL injection, solution, concentrate (intravenous) | Dopamine Hci | 6 products, 4 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Dopamine hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA018132 | Hospira | May 19, 1981 | 2 |
Companies that list Dopamine Hci
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Dopamine Hci products.
Recalls
No recall linked to Dopamine Hci products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.