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Heparin Sodium and Sodium Chloride - 0338-0433-04 - (HEPARIN SODIUM)

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Drug Information of Heparin Sodium and Sodium Chloride

Product NDC: 0338-0433
Proprietary Name: Heparin Sodium and Sodium Chloride
Non Proprietary Name: HEPARIN SODIUM
Active Ingredient(s): 2    [USP'U]/mL & nbsp;   HEPARIN SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Heparin Sodium and Sodium Chloride

Product NDC: 0338-0433
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018609
Marketing Category: NDA
Start Marketing Date: 19820428

Package Information of Heparin Sodium and Sodium Chloride

Package NDC: 0338-0433-04
Package Description: 12 BAG in 1 CARTON (0338-0433-04) > 1000 mL in 1 BAG

NDC Information of Heparin Sodium and Sodium Chloride

NDC Code 0338-0433-04
Proprietary Name Heparin Sodium and Sodium Chloride
Package Description 12 BAG in 1 CARTON (0338-0433-04) > 1000 mL in 1 BAG
Product NDC 0338-0433
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPARIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19820428
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name HEPARIN SODIUM
Strength Number 2
Strength Unit [USP'U]/mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium and Sodium Chloride


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