NDC 63323-915 – Heparin Sodium

Heparin Sodium 20000 [USP'U]/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug 1 recall

Product NDC63323-915

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
November 4, 2019
Listing expires
December 31, 2027
Pharmacologic class
Anti-coagulant; Unfractionated Heparin

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
63323-915-1325 VIAL in 1 TRAY (63323-915-13) / 1 mL in 1 VIAL (63323-915-03)Nov 4, 2019

Recalls mentioning this NDC

Other Heparin Sodium products