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CLADOSPORIUM FULVUM - 54575-192-02 - (passalora fulva)

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Drug Information of CLADOSPORIUM FULVUM

Product NDC: 54575-192
Proprietary Name: CLADOSPORIUM FULVUM
Non Proprietary Name: passalora fulva
Active Ingredient(s): 1    g/20mL & nbsp;   passalora fulva
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CLADOSPORIUM FULVUM

Product NDC: 54575-192
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of CLADOSPORIUM FULVUM

Package NDC: 54575-192-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-192-02)

NDC Information of CLADOSPORIUM FULVUM

NDC Code 54575-192-02
Proprietary Name CLADOSPORIUM FULVUM
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-192-02)
Product NDC 54575-192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name passalora fulva
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name PASSALORA FULVA
Strength Number 1
Strength Unit g/20mL
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 CLADOSPORIUM FULVUM


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