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NEUROSPORA INTERMEDIA - 0268-0917-10 - (NEUROSPORA INTERMEDIA)

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Drug Information of NEUROSPORA INTERMEDIA

Product NDC: 0268-0917
Proprietary Name: NEUROSPORA INTERMEDIA
Non Proprietary Name: NEUROSPORA INTERMEDIA
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   NEUROSPORA INTERMEDIA
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of NEUROSPORA INTERMEDIA

Product NDC: 0268-0917
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of NEUROSPORA INTERMEDIA

Package NDC: 0268-0917-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0917-10)

NDC Information of NEUROSPORA INTERMEDIA

NDC Code 0268-0917-10
Proprietary Name NEUROSPORA INTERMEDIA
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0917-10)
Product NDC 0268-0917
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name NEUROSPORA INTERMEDIA
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name NEUROSPORA INTERMEDIA
Strength Number 20000
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 NEUROSPORA INTERMEDIA


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