Fusarium - 49643-111-50 - (Fusarium solani)

Alphabetical Index


Drug Information of Fusarium

Product NDC: 49643-111
Proprietary Name: Fusarium
Non Proprietary Name: Fusarium solani
Active Ingredient(s): 1    g/10mL & nbsp;   Fusarium solani
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fusarium

Product NDC: 49643-111
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Fusarium

Package NDC: 49643-111-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49643-111-50)

NDC Information of Fusarium

NDC Code 49643-111-50
Proprietary Name Fusarium
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49643-111-50)
Product NDC 49643-111
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Fusarium solani
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name HAEMATONECTRIA HAEMATOCOCCA
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Fusarium


General Information