NDC 0409-2222 – Heparin Sodium

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

Human Prescription Drug 3 recalls

Product NDC0409-2222

Product details

Brand name
Heparin Sodium
Generic name
Heparin Sodium
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA018916
Marketed since
February 27, 2023
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
0409-2222-1212 POUCH in 1 CASE (0409-2222-12) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-2222-01)Feb 27, 2023

Recalls mentioning this NDC

Other Heparin Sodium products