Product NDC: | 0517-1130 |
Proprietary Name: | Epinephrine |
Non Proprietary Name: | Epinephrine |
Active Ingredient(s): | 1 mg/mL & nbsp; Epinephrine |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-1130 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19940301 |
Package NDC: | 0517-1130-05 |
Package Description: | 5 VIAL, MULTI-DOSE in 1 CARTON (0517-1130-05) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0517-1130-05 |
Proprietary Name | Epinephrine |
Package Description | 5 VIAL, MULTI-DOSE in 1 CARTON (0517-1130-05) > 30 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 0517-1130 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Epinephrine |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 19940301 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | American Regent, 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] |