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Epinephrine - 0409-4921-34 - (EPINEPHRINE)

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Drug Information of Epinephrine

Product NDC: 0409-4921
Proprietary Name: Epinephrine
Non Proprietary Name: EPINEPHRINE
Active Ingredient(s): .1    mg/mL & nbsp;   EPINEPHRINE
Administration Route(s): ENDOTRACHEAL; INTRACARDIAC; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Epinephrine

Product NDC: 0409-4921
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19850405

Package Information of Epinephrine

Package NDC: 0409-4921-34
Package Description: 10 CARTON in 1 PACKAGE (0409-4921-34) > 1 SYRINGE in 1 CARTON > 10 mL in 1 SYRINGE

NDC Information of Epinephrine

NDC Code 0409-4921-34
Proprietary Name Epinephrine
Package Description 10 CARTON in 1 PACKAGE (0409-4921-34) > 1 SYRINGE in 1 CARTON > 10 mL in 1 SYRINGE
Product NDC 0409-4921
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPINEPHRINE
Dosage Form Name INJECTION, SOLUTION
Route Name ENDOTRACHEAL; INTRACARDIAC; INTRAVENOUS
Start Marketing Date 19850405
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]

Complete Information of Epinephrine


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