NDC 0409-1775 – Dextrose

Dextrose Monohydrate 250 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 2 recalls

Product NDC0409-1775

Product details

Brand name
Dextrose
Generic name
Dextrose monohydrate
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA019445
Marketed since
February 22, 2006
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Dextrose →

Package NDC codes (1)

Package NDCDescriptionSince
0409-1775-1010 CARTON in 1 PACKAGE (0409-1775-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40)Feb 22, 2006

Recalls mentioning this NDC

Other Dextrose products