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FAGUS GRANDIFOLIA POLLEN - 0268-6684-05 - (Beech)

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Drug Information of FAGUS GRANDIFOLIA POLLEN

Product NDC: 0268-6684
Proprietary Name: FAGUS GRANDIFOLIA POLLEN
Non Proprietary Name: Beech
Active Ingredient(s): 1000    [PNU]/mL & nbsp;   Beech
Administration Route(s): INTRADERMAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FAGUS GRANDIFOLIA POLLEN

Product NDC: 0268-6684
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of FAGUS GRANDIFOLIA POLLEN

Package NDC: 0268-6684-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6684-05)

NDC Information of FAGUS GRANDIFOLIA POLLEN

NDC Code 0268-6684-05
Proprietary Name FAGUS GRANDIFOLIA POLLEN
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6684-05)
Product NDC 0268-6684
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Beech
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name FAGUS GRANDIFOLIA POLLEN
Strength Number 1000
Strength Unit [PNU]/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 FAGUS GRANDIFOLIA POLLEN


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