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EPICOCCUM NIGRUM - 0268-0892-10 - (EPICOCCUM NIGRUM)

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Drug Information of EPICOCCUM NIGRUM

Product NDC: 0268-0892
Proprietary Name: EPICOCCUM NIGRUM
Non Proprietary Name: EPICOCCUM NIGRUM
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   EPICOCCUM NIGRUM
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of EPICOCCUM NIGRUM

Product NDC: 0268-0892
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of EPICOCCUM NIGRUM

Package NDC: 0268-0892-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0892-10)

NDC Information of EPICOCCUM NIGRUM

NDC Code 0268-0892-10
Proprietary Name EPICOCCUM NIGRUM
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0892-10)
Product NDC 0268-0892
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name EPICOCCUM NIGRUM
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name EPICOCCUM NIGRUM
Strength Number 20000
Strength Unit [PNU]/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 NIGRUM


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