NDC 63323-262 – Heparin Sodium

Heparin Sodium 5000 [USP'U]/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug 1 recall

Product NDC63323-262

Product details

Brand name
Heparin Sodium
Generic name
Heparin Sodium
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Marketing category
NDA · NDA017029
Marketed since
March 2, 2020
Listing expires
December 31, 2026
Pharmacologic class
Anti-coagulant; Unfractionated Heparin

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
63323-262-0625 VIAL in 1 TRAY (63323-262-06) / 1 mL in 1 VIAL (63323-262-03)Mar 25, 2020
63323-262-2625 VIAL in 1 TRAY (63323-262-26) / 1 mL in 1 VIAL (63323-262-09)Mar 25, 2020
63323-262-3625 VIAL in 1 TRAY (63323-262-36) / 1 mL in 1 VIAL (63323-262-11)Mar 2, 2020

Recalls mentioning this NDC

Other Heparin Sodium products