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Heparin Sodium - 0069-0043-01 - (Heparin Sodium)

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Drug Information of Heparin Sodium

Product NDC: 0069-0043
Proprietary Name: Heparin Sodium
Non Proprietary Name: Heparin Sodium
Active Ingredient(s): 1000    [USP'U]/mL & nbsp;   Heparin Sodium
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Heparin Sodium

Product NDC: 0069-0043
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA201370
Marketing Category: NDA
Start Marketing Date: 20110721

Package Information of Heparin Sodium

Package NDC: 0069-0043-01
Package Description: 25 VIAL in 1 CONTAINER (0069-0043-01) > 2 mL in 1 VIAL (0069-0043-02)

NDC Information of Heparin Sodium

NDC Code 0069-0043-01
Proprietary Name Heparin Sodium
Package Description 25 VIAL in 1 CONTAINER (0069-0043-01) > 2 mL in 1 VIAL (0069-0043-02)
Product NDC 0069-0043
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Heparin Sodium
Dosage Form Name INJECTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110721
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name HEPARIN SODIUM
Strength Number 1000
Strength Unit [USP'U]/mL
Pharmaceutical Classes Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC]

Complete Information of Heparin Sodium


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