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Fusarium compactum - 36987-1978-1 - (Fusarium compactum)

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Drug Information of Fusarium compactum

Product NDC: 36987-1978
Proprietary Name: Fusarium compactum
Non Proprietary Name: Fusarium compactum
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Fusarium compactum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fusarium compactum

Product NDC: 36987-1978
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Fusarium compactum

Package NDC: 36987-1978-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-1978-1)

NDC Information of Fusarium compactum

NDC Code 36987-1978-1
Proprietary Name Fusarium compactum
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-1978-1)
Product NDC 36987-1978
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fusarium compactum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name FUSARIUM COMPACTUM
Strength Number 40000
Strength Unit [PNU]/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 Fusarium compactum


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