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Norepinephrine bitartrate
Norepinephrine bitartrate - 0703-1153-03 - (Norepinephrine bitartrate)
Drug Information of Norepinephrine bitartrate
| Product NDC: | 0703-1153 |
| Proprietary Name: | Norepinephrine bitartrate |
| 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 bitartrate
| Product NDC: | 0703-1153 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040455 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030401 |
Package Information of Norepinephrine bitartrate
| Package NDC: | 0703-1153-03 |
| Package Description: | 10 VIAL in 1 TRAY (0703-1153-03) > 4 mL in 1 VIAL (0703-1153-01) |
NDC Information of Norepinephrine bitartrate
| NDC Code | 0703-1153-03 |
| Proprietary Name | Norepinephrine bitartrate |
| Package Description | 10 VIAL in 1 TRAY (0703-1153-03) > 4 mL in 1 VIAL (0703-1153-01) |
| Product NDC | 0703-1153 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norepinephrine bitartrate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030401 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | NOREPINEPHRINE BITARTRATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
