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Epicoccum nigrum - 36987-1972-4 - (Epicoccum nigrum)

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Drug Information of Epicoccum nigrum

Product NDC: 36987-1972
Proprietary Name: Epicoccum nigrum
Non Proprietary Name: Epicoccum nigrum
Active Ingredient(s): .1    g/mL & nbsp;   Epicoccum nigrum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Epicoccum nigrum

Product NDC: 36987-1972
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Epicoccum nigrum

Package NDC: 36987-1972-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1972-4)

NDC Information of Epicoccum nigrum

NDC Code 36987-1972-4
Proprietary Name Epicoccum nigrum
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1972-4)
Product NDC 36987-1972
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epicoccum nigrum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name EPICOCCUM NIGRUM
Strength Number .1
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 nigrum


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