Product NDC: | 49349-747 |
Proprietary Name: | EpiPen |
Non Proprietary Name: | Epinephrine |
Active Ingredient(s): | .3 mg/.3mL & nbsp; Epinephrine |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-747 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019430 |
Marketing Category: | NDA |
Start Marketing Date: | 20130611 |
Package NDC: | 49349-747-01 |
Package Description: | .3 mL in 1 SYRINGE, GLASS (49349-747-01) |
NDC Code | 49349-747-01 |
Proprietary Name | EpiPen |
Package Description | .3 mL in 1 SYRINGE, GLASS (49349-747-01) |
Product NDC | 49349-747 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Epinephrine |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20130611 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | EPINEPHRINE |
Strength Number | .3 |
Strength Unit | mg/.3mL |
Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |