NDC 25021-404 – Heparin Sodium

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

Human Prescription Drug 1 recall

Product NDC25021-404

Product details

Brand name
Heparin Sodium
Generic name
Heparin sodium
Labeler
Sagent Pharmaceuticals
Dosage form
Injection
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA090809
Marketed since
July 6, 2010
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
25021-404-0125 VIAL in 1 CARTON (25021-404-01) / 1 mL in 1 VIALJul 6, 2010

Recalls mentioning this NDC

Other Heparin Sodium products