NDC 51662-1337 – Dobutamine

Dobutamine Hydrochloride 12.5 mg/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC51662-1337

Product details

Brand name
Dobutamine
Generic name
Dobutamine
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA074086
Marketed since
November 26, 2018
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Dobutamine →

Package NDC codes (2)

Package NDCDescriptionSince
51662-1337-120 mL in 1 VIAL, SINGLE-DOSE (51662-1337-1)Nov 26, 2018
51662-1337-310 POUCH in 1 CASE (51662-1337-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1337-2) / 20 mL in 1 VIAL, SINGLE-DOSEJun 12, 2022

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