NDC 71288-402 – Heparin Sodium

Heparin Sodium 1000 [USP'U]/mL · Injection · Intravenous, Subcutaneous

Human Prescription Drug

Product NDC71288-402

Product details

Brand name
Heparin Sodium
Generic name
Heparin Sodium
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
Injection
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA211007
Marketed since
June 15, 2019
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
71288-402-0225 VIAL, SINGLE-DOSE in 1 CARTON (71288-402-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-402-01)Jun 15, 2019
71288-402-1125 VIAL, MULTI-DOSE in 1 CARTON (71288-402-11) / 10 mL in 1 VIAL, MULTI-DOSE (71288-402-10)Jun 15, 2019
71288-402-3125 VIAL, MULTI-DOSE in 1 CARTON (71288-402-31) / 30 mL in 1 VIAL, MULTI-DOSE (71288-402-30)Jun 15, 2019

Other Heparin Sodium products