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KOCHIA SCOPARIA POLLEN - 0268-1232-50 - (Kochia Firebush)

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Drug Information of KOCHIA SCOPARIA POLLEN

Product NDC: 0268-1232
Proprietary Name: KOCHIA SCOPARIA POLLEN
Non Proprietary Name: Kochia Firebush
Active Ingredient(s): .1    g/mL & nbsp;   Kochia Firebush
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of KOCHIA SCOPARIA POLLEN

Product NDC: 0268-1232
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of KOCHIA SCOPARIA POLLEN

Package NDC: 0268-1232-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-1232-50)

NDC Information of KOCHIA SCOPARIA POLLEN

NDC Code 0268-1232-50
Proprietary Name KOCHIA SCOPARIA POLLEN
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-1232-50)
Product NDC 0268-1232
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Kochia Firebush
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name KOCHIA SCOPARIA POLLEN
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of KOCHIA SCOPARIA POLLEN


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