NDC 0338-0017 – Dextrose

Dextrose Monohydrate 50 g/1000mL · Injection, Solution · Intravenous

Human Prescription Drug 6 recalls

Product NDC0338-0017

Product details

Brand name
Dextrose
Generic name
Dextrose Monohydrate
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA016673
Marketed since
March 4, 1971
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Dextrose →

Package NDC codes (10)

Package NDCDescriptionSince
0338-0017-02250 mL in 1 BAG (0338-0017-02)Mar 4, 1971
0338-0017-03500 mL in 1 BAG (0338-0017-03)Mar 4, 1971
0338-0017-041000 mL in 1 BAG (0338-0017-04)Mar 4, 1971
0338-0017-104 BAG in 1 POUCH (0338-0017-10) / 25 mL in 1 BAGMar 4, 1971
0338-0017-114 BAG in 1 POUCH (0338-0017-11) / 50 mL in 1 BAGMar 4, 1971
0338-0017-184 BAG in 1 POUCH (0338-0017-18) / 100 mL in 1 BAGMar 4, 1971
0338-0017-3116 BAG in 1 POUCH (0338-0017-31) / 50 mL in 1 BAGMar 4, 1971
0338-0017-3816 BAG in 1 POUCH (0338-0017-38) / 100 mL in 1 BAGMar 4, 1971
0338-0017-411 BAG in 1 PACKAGE (0338-0017-41) / 50 mL in 1 BAGMar 4, 1971
0338-0017-481 BAG in 1 PACKAGE (0338-0017-48) / 100 mL in 1 BAGMar 4, 1971

Recalls mentioning this NDC

Other Dextrose products