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INNOHEP
INNOHEP - 50222-342-53 - (tinzaparin sodium)
Drug Information of INNOHEP
| Product NDC: | 50222-342 |
| Proprietary Name: | INNOHEP |
| Non Proprietary Name: | tinzaparin sodium |
| Active Ingredient(s): | 20000 [iU]/mL & nbsp; tinzaparin sodium |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of INNOHEP
| Product NDC: | 50222-342 |
| Labeler Name: | LEO Pharma Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020484 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100701 |
Package Information of INNOHEP
| Package NDC: | 50222-342-53 |
| Package Description: | 10 VIAL, MULTI-DOSE in 1 CARTON (50222-342-53) > 2 mL in 1 VIAL, MULTI-DOSE |
NDC Information of INNOHEP
| NDC Code | 50222-342-53 |
| Proprietary Name | INNOHEP |
| Package Description | 10 VIAL, MULTI-DOSE in 1 CARTON (50222-342-53) > 2 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 50222-342 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tinzaparin sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20100701 |
| Marketing Category Name | NDA |
| Labeler Name | LEO Pharma Inc. |
| Substance Name | TINZAPARIN SODIUM |
| Strength Number | 20000 |
| Strength Unit | [iU]/mL |
| Pharmaceutical Classes | Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |
