NDC 0338-0428 – Heparin Sodium In Sodium Chloride

Heparin Sodium 200 [USP'U]/100mL · Injection, Solution · Intravenous

Human Prescription Drug 4 recalls

Product NDC0338-0428

Product details

Brand name
Heparin Sodium In Sodium Chloride
Generic name
Heparin Sodium
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA018609
Marketed since
April 28, 1982
Listing expires
December 31, 2027
Pharmacologic class
Anti-coagulant; Unfractionated Heparin

Active ingredients

Uses, dosage, side effects and warnings for Heparin Sodium in Sodium Chloride →

Package NDC codes (1)

Package NDCDescriptionSince
0338-0428-1212 BAG in 1 CARTON (0338-0428-12) / 1000 mL in 1 BAGApr 23, 2020

Recalls mentioning this NDC

Other Heparin Sodium in Sodium Chloride products