NDC 0338-0719 – Dextrose

Dextrose Monohydrate 70 g/100mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0338-0719

Product details

Brand name
Dextrose
Generic name
Dextrose monohydrate
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA020047
Marketed since
July 2, 1991
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Dextrose →

Package NDC codes (1)

Package NDCDescriptionSince
0338-0719-062000 mL in 1 BAG (0338-0719-06)Jul 2, 1991

Recalls mentioning this NDC

Other Dextrose products