United States · FDA National Drug Code directory

Dobutamine Hydrochloride in Dextrose

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0338-1075_34c787c1-46f7-4264-951d-c88a34dca533
Product NDC
0338-1075
Form
INJECTION
Composition / generic term
Dobutamine Hydrochloride
Labeler
Baxter Healthcare Corporation
Marketing category
NDA
Marketing start / end (source format)
19930927
Source listing expiry
20271231

Source-listed ingredients

  • DOBUTAMINE HYDROCHLORIDE — 200 mg/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 18 BAG in 1 CARTON (0338-1075-02) / 250 mL in 1 BAG · 0338-1075-02

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →