Adrenalin - 42023-159-25 - (epinephrine)

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Drug Information of Adrenalin

Product NDC: 42023-159
Proprietary Name: Adrenalin
Non Proprietary Name: epinephrine
Active Ingredient(s): 1    mg/mL & nbsp;   epinephrine
Administration Route(s): INTRAMUSCULAR; INTRAOCULAR; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Adrenalin

Product NDC: 42023-159
Labeler Name: JHP Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA204200
Marketing Category: NDA
Start Marketing Date: 20130701

Package Information of Adrenalin

Package NDC: 42023-159-25
Package Description: 25 VIAL in 1 CARTON (42023-159-25) > 1 mL in 1 VIAL

NDC Information of Adrenalin

NDC Code 42023-159-25
Proprietary Name Adrenalin
Package Description 25 VIAL in 1 CARTON (42023-159-25) > 1 mL in 1 VIAL
Product NDC 42023-159
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name epinephrine
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAOCULAR; SUBCUTANEOUS
Start Marketing Date 20130701
Marketing Category Name NDA
Labeler Name JHP Pharmaceuticals LLC
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 Adrenalin


General Information