Heparin Sodium 71839-0117-25

Package NDC

71839-0117-25

Manufacturer: Be Pharmaceuticals Inc.
Dosage Form: Injection, Solution
Route: Intravenous And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: December 29, 2020
Listing Expires: December 31, 2026
Application: ANDA214804

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Active Ingredients

Ingredient	Strength
Heparin Sodium	2000 [USP'U]/2mL

Drug Class

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

Selected Package

71839-0117-25Selected

25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01)