Heparin Sodium In Sodium Chloride 51662-1578-01

Package NDC

51662-1578-01

Manufacturer: Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: July 15, 2021
Listing Expires: December 31, 2026
Application: NDA017029

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Active Ingredients

Ingredient	Strength
Heparin Sodium	10000 [USP'U]/100mL

Drug Class

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

Selected Package

51662-1578-01Selected

250 mL in 1 BAG (51662-1578-1)