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Epinephrine
Epinephrine - 0409-7241-61 - (EPINEPHRINE)
Drug Information of Epinephrine
| Product NDC: | 0409-7241 |
| Proprietary Name: | Epinephrine |
| Non Proprietary Name: | EPINEPHRINE |
| Active Ingredient(s): | 1 mg/mL & nbsp; EPINEPHRINE |
| Administration Route(s): | INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Epinephrine
| Product NDC: | 0409-7241 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20050908 |
Package Information of Epinephrine
| Package NDC: | 0409-7241-61 |
| Package Description: | 800 AMPULE in 1 CASE (0409-7241-61) > 1 mL in 1 AMPULE |
NDC Information of Epinephrine
| NDC Code | 0409-7241-61 |
| Proprietary Name | Epinephrine |
| Package Description | 800 AMPULE in 1 CASE (0409-7241-61) > 1 mL in 1 AMPULE |
| Product NDC | 0409-7241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EPINEPHRINE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20050908 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Hospira, Inc. |
| Substance Name | EPINEPHRINE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
