Heparin Sodium 00409-1316-32

Package NDC

00409-1316-32

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution
Route: Intravenous And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: March 31, 2005
Listing Expires: December 31, 2027
Application: ANDA089522

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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

00409-1316-32Selected

50 CARTRIDGE in 1 CONTAINER (0409-1316-32) / .5 mL in 1 CARTRIDGE (0409-1316-11)