NDC 0338-0023 – Dextrose

Dextrose Monohydrate 100 g/1000mL · Injection, Solution · Intravenous

Human Prescription Drug 6 recalls

Product NDC0338-0023

Product details

Brand name
Dextrose
Generic name
Dextrose Monohydrate
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA016694
Marketed since
January 25, 1971
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Dextrose →

Package NDC codes (3)

Package NDCDescriptionSince
0338-0023-02250 mL in 1 BAG (0338-0023-02)Jan 25, 1971
0338-0023-03500 mL in 1 BAG (0338-0023-03)Jan 25, 1971
0338-0023-041000 mL in 1 BAG (0338-0023-04)Jan 25, 1971

Recalls mentioning this NDC

Other Dextrose products