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Heparin Sodium
Heparin Sodium - 0409-1316-32 - (HEPARIN SODIUM)
Drug Information of Heparin Sodium
| Product NDC: | 0409-1316 |
| Proprietary Name: | Heparin Sodium |
| Non Proprietary Name: | HEPARIN SODIUM |
| Active Ingredient(s): | 10000 [USP'U]/mL & nbsp; HEPARIN SODIUM |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium
| Product NDC: | 0409-1316 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089522 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870504 |
Package Information of Heparin Sodium
| Package NDC: | 0409-1316-32 |
| Package Description: | 50 CARTRIDGE in 1 CONTAINER (0409-1316-32) > .5 mL in 1 CARTRIDGE |
NDC Information of Heparin Sodium
| NDC Code | 0409-1316-32 |
| Proprietary Name | Heparin Sodium |
| Package Description | 50 CARTRIDGE in 1 CONTAINER (0409-1316-32) > .5 mL in 1 CARTRIDGE |
| Product NDC | 0409-1316 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HEPARIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19870504 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 10000 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
