Drug
Who makes dobutamine?
4 companies list dobutamine as a human prescription drug. Forms: injection; injection, solution; injection, solution, concentrate. Routes: intravenous.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing dobutamine
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| HF Acquisition Co LLCUnited States | injection, solution; injection, solution, concentrate | ANDA, NDAANDA074086, NDA020201 | 2 | 1 |
| Hospira, Inc.United States | injection, solution, concentrate | ANDAANDA074086 | 1 | 7 |
| Hikma Pharmaceuticals USA Inc.United States | injection, solution | ANDAANDA074277 | 1 | 4 |
| Slate Run Pharmaceuticals, LLCUnited States | injection | ANDAANDA216131 | 1 | 1 |
Enquiry
Common questions
- Who makes dobutamine?
- 4 companies list dobutamine as a human prescription drug in the openFDA NDC Directory, led by HF Acquisition Co LLC, Hospira, Inc., Hikma Pharmaceuticals USA Inc., Slate Run Pharmaceuticals, LLC. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic dobutamine?
- 4 companies list dobutamine under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.