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EPINEPHRINE - 54868-6239-1 - (epinephrine)

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Drug Information of EPINEPHRINE

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)

Labeler Information of EPINEPHRINE

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 Information of EPINEPHRINE

Package NDC: 54868-6239-1
Package Description: 1 CARTRIDGE in 1 CASE (54868-6239-1) > 1 INJECTION in 1 CARTRIDGE

NDC Information of EPINEPHRINE

NDC Code 54868-6239-1
Proprietary Name EPINEPHRINE
Package Description 1 CARTRIDGE in 1 CASE (54868-6239-1) > 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]

Complete Information of EPINEPHRINE


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