NDC 0338-0126 – Myxredlin

Insulin Human 1 [iU]/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0338-0126

Product details

Brand name
Myxredlin
Generic name
Insulin human
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
BLA · BLA208157
Marketed since
July 12, 2019
Listing expires
December 31, 2027
Pharmacologic class
Insulin

Active ingredients

Uses, dosage, side effects and warnings for Myxredlin →

Package NDC codes (1)

Package NDCDescriptionSince
0338-0126-1212 CONTAINER in 1 CARTON (0338-0126-12) / 100 mL in 1 CONTAINERJul 12, 2019

Recalls mentioning this NDC