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HOUSEFLY FOR DIAGNOSTIC USE ONLY - 54575-321-30 - (musca domestica)

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Drug Information of HOUSEFLY FOR DIAGNOSTIC USE ONLY

Product NDC: 54575-321
Proprietary Name: HOUSEFLY FOR DIAGNOSTIC USE ONLY
Non Proprietary Name: musca domestica
Active Ingredient(s): 1    g/50mL & nbsp;   musca domestica
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HOUSEFLY FOR DIAGNOSTIC USE ONLY

Product NDC: 54575-321
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of HOUSEFLY FOR DIAGNOSTIC USE ONLY

Package NDC: 54575-321-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (54575-321-30)

NDC Information of HOUSEFLY FOR DIAGNOSTIC USE ONLY

NDC Code 54575-321-30
Proprietary Name HOUSEFLY FOR DIAGNOSTIC USE ONLY
Package Description 30 mL in 1 VIAL, MULTI-DOSE (54575-321-30)
Product NDC 54575-321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name musca domestica
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name MUSCA DOMESTICA
Strength Number 1
Strength Unit g/50mL
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 HOUSEFLY FOR DIAGNOSTIC USE ONLY


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