Product NDC: | 0069-0059 |
Proprietary Name: | Heparin Sodium |
Non Proprietary Name: | Heparin Sodium |
Active Ingredient(s): | 5000 [USP'U]/mL & nbsp; Heparin Sodium |
Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0059 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA201370 |
Marketing Category: | NDA |
Start Marketing Date: | 20110721 |
Package NDC: | 0069-0059-02 |
Package Description: | 10 mL in 1 VIAL (0069-0059-02) |
NDC Code | 0069-0059-02 |
Proprietary Name | Heparin Sodium |
Package Description | 10 mL in 1 VIAL (0069-0059-02) |
Product NDC | 0069-0059 |
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 | 5000 |
Strength Unit | [USP'U]/mL |
Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |