Heparin Sodium 00781-3439-25

Package NDC

00781-3439-25

Manufacturer: Sandoz Inc.
Dosage Form: Injection, Solution
Route: Intravenous And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: June 12, 2014
Listing Expires: December 31, 2026
Application: ANDA203198

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Active Ingredients

Ingredient	Strength
Heparin Sodium	10000 [USP'U]/mL

Drug Class

Anti-coagulant [EPC]Heparin [CS]Unfractionated Heparin [EPC]

Selected Package

00781-3439-25Selected

25 VIAL, MULTI-DOSE in 1 CARTON (0781-3439-25) / 1 mL in 1 VIAL, MULTI-DOSE (0781-3439-10)