Epicoccum - 49288-0187-1 - (Epicoccum)

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Drug Information of Epicoccum

Product NDC: 49288-0187
Proprietary Name: Epicoccum
Non Proprietary Name: Epicoccum
Active Ingredient(s): .05    g/mL & nbsp;   Epicoccum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Epicoccum

Product NDC: 49288-0187
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Epicoccum

Package NDC: 49288-0187-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0187-1)

NDC Information of Epicoccum

NDC Code 49288-0187-1
Proprietary Name Epicoccum
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0187-1)
Product NDC 49288-0187
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epicoccum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name EPICOCCUM NIGRUM
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE]

Complete Information of Epicoccum


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