Home > National Drug Code (NDC) > CLADOSPORIUM CLADOSPORIOIDES

CLADOSPORIUM CLADOSPORIOIDES - 0268-0859-50 - (CLADOSPORIUM CLADOSPORIOIDES)

Alphabetical Index


Drug Information of CLADOSPORIUM CLADOSPORIOIDES

Product NDC: 0268-0859
Proprietary Name: CLADOSPORIUM CLADOSPORIOIDES
Non Proprietary Name: CLADOSPORIUM CLADOSPORIOIDES
Active Ingredient(s): .01    g/mL & nbsp;   CLADOSPORIUM CLADOSPORIOIDES
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CLADOSPORIUM CLADOSPORIOIDES

Product NDC: 0268-0859
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of CLADOSPORIUM CLADOSPORIOIDES

Package NDC: 0268-0859-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0859-50)

NDC Information of CLADOSPORIUM CLADOSPORIOIDES

NDC Code 0268-0859-50
Proprietary Name CLADOSPORIUM CLADOSPORIOIDES
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0859-50)
Product NDC 0268-0859
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name CLADOSPORIUM CLADOSPORIOIDES
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name CLADOSPORIUM CLADOSPORIOIDES
Strength Number .01
Strength Unit g/mL
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 CLADOSPORIOIDES


General Information