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BETULA LENTA POLLEN - 0268-6686-05 - (Black Birch)

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Drug Information of BETULA LENTA POLLEN

Product NDC: 0268-6686
Proprietary Name: BETULA LENTA POLLEN
Non Proprietary Name: Black Birch
Active Ingredient(s): 1000    [PNU]/mL & nbsp;   Black Birch
Administration Route(s): INTRADERMAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BETULA LENTA POLLEN

Product NDC: 0268-6686
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of BETULA LENTA POLLEN

Package NDC: 0268-6686-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6686-05)

NDC Information of BETULA LENTA POLLEN

NDC Code 0268-6686-05
Proprietary Name BETULA LENTA POLLEN
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6686-05)
Product NDC 0268-6686
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Black Birch
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name BETULA LENTA 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 BETULA LENTA POLLEN


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