United States · FDA National Drug Code directory

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
0409-1775_8ef5055d-1ca7-42b8-81bd-ecfcf303173b
Product NDC
0409-1775
Form
INJECTION, SOLUTION
Composition / generic term
Dextrose monohydrate
Labeler
Hospira, Inc.
Marketing category
NDA
Marketing start / end (source format)
20060222
Source listing expiry
20271231

Source-listed ingredients

  • DEXTROSE MONOHYDRATE — 250 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 CARTON in 1 PACKAGE (0409-1775-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40) · 0409-1775-10

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 →