NDC 51662-1705
Dobutamine In Dextrose 200 mg per 100 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-0151.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hospira, Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Dobutamine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 200 mg per 100 mL
- Approval
- NDA NDA020201
- On the market since
- Mar 16, 2026
- Package NDCs
51662-1705-1- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2026
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