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Norepinephrine
Norepinephrine - 55390-002-10 - (Norepinephrine bitartrate)
Drug Information of Norepinephrine
| Product NDC: | 55390-002 |
| Proprietary Name: | Norepinephrine |
| Non Proprietary Name: | Norepinephrine bitartrate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Norepinephrine bitartrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Norepinephrine
| Product NDC: | 55390-002 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040462 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031117 |
Package Information of Norepinephrine
| Package NDC: | 55390-002-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-002-10) > 4 mL in 1 VIAL |
NDC Information of Norepinephrine
| NDC Code | 55390-002-10 |
| Proprietary Name | Norepinephrine |
| Package Description | 10 VIAL in 1 BOX (55390-002-10) > 4 mL in 1 VIAL |
| Product NDC | 55390-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norepinephrine bitartrate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20031117 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | NOREPINEPHRINE BITARTRATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
