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Humicola grisea - 49288-0635-4 - (Humicola grisea)

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Drug Information of Humicola grisea

Product NDC: 49288-0635
Proprietary Name: Humicola grisea
Non Proprietary Name: Humicola grisea
Active Ingredient(s): .05    g/mL & nbsp;   Humicola grisea
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Humicola grisea

Product NDC: 49288-0635
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Humicola grisea

Package NDC: 49288-0635-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0635-4)

NDC Information of Humicola grisea

NDC Code 49288-0635-4
Proprietary Name Humicola grisea
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0635-4)
Product NDC 49288-0635
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Humicola grisea
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name HUMICOLA GRISEA
Strength Number .05
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 Humicola grisea


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