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NITROPRESS
NITROPRESS - 0409-3024-01 - (SODIUM NITROPRUSSIDE)
Drug Information of NITROPRESS
| Product NDC: | 0409-3024 |
| Proprietary Name: | NITROPRESS |
| Non Proprietary Name: | SODIUM NITROPRUSSIDE |
| Active Ingredient(s): | 50 mg/2mL & nbsp; SODIUM NITROPRUSSIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NITROPRESS
| Product NDC: | 0409-3024 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071961 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091019 |
Package Information of NITROPRESS
| Package NDC: | 0409-3024-01 |
| Package Description: | 1 VIAL in 1 CARTON (0409-3024-01) > 2 mL in 1 VIAL |
NDC Information of NITROPRESS
| NDC Code | 0409-3024-01 |
| Proprietary Name | NITROPRESS |
| Package Description | 1 VIAL in 1 CARTON (0409-3024-01) > 2 mL in 1 VIAL |
| Product NDC | 0409-3024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM NITROPRUSSIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091019 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM NITROPRUSSIDE |
| Strength Number | 50 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes |
