Product NDC: | 54868-6239 |
Proprietary Name: | EPINEPHRINE |
Non Proprietary Name: | epinephrine |
Active Ingredient(s): | .3 mg/1 & nbsp; epinephrine |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6239 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020800 |
Marketing Category: | NDA |
Start Marketing Date: | 20110418 |
Package NDC: | 54868-6239-0 |
Package Description: | 2 CARTRIDGE in 1 CASE (54868-6239-0) > 1 INJECTION in 1 CARTRIDGE |
NDC Code | 54868-6239-0 |
Proprietary Name | EPINEPHRINE |
Package Description | 2 CARTRIDGE in 1 CASE (54868-6239-0) > 1 INJECTION in 1 CARTRIDGE |
Product NDC | 54868-6239 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | epinephrine |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 20110418 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | EPINEPHRINE |
Strength Number | .3 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |