NDC 51662-1566

Dobutamine Hydrochloride 100 mg per 100 mL injection

On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Baxter Healthcare Corporation's NDC 0338-1073.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Baxter Healthcare CorporationJayuya, PR, United StatesMakes it, tests it, packages it, labels it and sterilizes it Problems found, fixed voluntarilyJul 19, 2024 · 15 inspections, 5 with FDA action
Baxter Healthcare CorporationRound Lake, IL, United StatesTests it Serious problems, FDA actionApr 2, 2026 · 15 inspections, 2 with FDA action

Repackaging site

Product details

Generic drug
Dobutamine: every company that makes it
Form
injection, intravenous
Strength
100 mg per 100 mL
Approval
NDA NDA020255
On the market since
Jul 10, 2021
Package NDCs
51662-1566-1
Official label
DailyMed (National Library of Medicine), updated Jan 30, 2024

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