| Product NDC: | 52533-100 | 
| Proprietary Name: | Heparin Sodium | 
| Non Proprietary Name: | Heparin Sodium | 
| Active Ingredient(s): | 1 [USP'U]/mL & nbsp; Heparin Sodium | 
| Administration Route(s): | INTRAVENOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 52533-100 | 
| Labeler Name: | Cantrell Drug Company | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20110222 | 
| Package NDC: | 52533-100-18 | 
| Package Description: | 250 mL in 1 BAG (52533-100-18) | 
| NDC Code | 52533-100-18 | 
| Proprietary Name | Heparin Sodium | 
| Package Description | 250 mL in 1 BAG (52533-100-18) | 
| Product NDC | 52533-100 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Heparin Sodium | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 20110222 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Cantrell Drug Company | 
| Substance Name | HEPARIN SODIUM | 
| Strength Number | 1 | 
| Strength Unit | [USP'U]/mL | 
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |