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Epinephrine - 0409-7241-61 - (EPINEPHRINE)

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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]

Complete Information of Epinephrine


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