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MOSQUITO FOR DIAGNOSTIC USE ONLY - 54575-324-50 - (aedes taeniorhynchus)

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Drug Information of MOSQUITO FOR DIAGNOSTIC USE ONLY

Product NDC: 54575-324
Proprietary Name: MOSQUITO FOR DIAGNOSTIC USE ONLY
Non Proprietary Name: aedes taeniorhynchus
Active Ingredient(s): 1    g/20mL & nbsp;   aedes taeniorhynchus
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MOSQUITO FOR DIAGNOSTIC USE ONLY

Product NDC: 54575-324
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of MOSQUITO FOR DIAGNOSTIC USE ONLY

Package NDC: 54575-324-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-324-50)

NDC Information of MOSQUITO FOR DIAGNOSTIC USE ONLY

NDC Code 54575-324-50
Proprietary Name MOSQUITO FOR DIAGNOSTIC USE ONLY
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-324-50)
Product NDC 54575-324
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name aedes taeniorhynchus
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name AEDES TAENIORHYNCHUS
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of MOSQUITO FOR DIAGNOSTIC USE ONLY


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