DOBUTAMINE IN DEXTROSE

NDC 51662-1697 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameDOBUTAMINE IN DEXTROSE

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)DOBUTAMINE HYDROCHLORIDE

Strength100 mg/100mL

Pharmacologic classAdrenergic beta-Agonists [MoA], beta-Adrenergic Agonist [EPC]

Marketing categoryNDA

Packages

51662-1697-1 — 250 mL in 1 BAG (51662-1697-1)

FDA lists these products with the same active ingredient.

0143-9141 — Dobutamine, 0338-1073 — Dobutamine Hydrochloride, 0338-1075 — Dobutamine Hydrochloride, 0338-1077 — Dobutamine Hydrochloride, 0409-0025 — Dobutamine in Dextrose, 0409-0151 — Dobutamine in Dextrose, 0409-1100 — Dobutamine in Dextrose, 0409-2344 — DOBUTAMINE, 51662-1330 — DOBUTAMINE, 51662-1337 — DOBUTAMINE, 51662-1566 — DOBUTAMINE HYDROCHLORIDE, 51662-1664 — DOBUTAMINE IN DEXTROSE, 51662-1705 — DOBUTAMINE IN DEXTROSE, 70436-203 — dobutamine

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.