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POPULUS TREMULOIDES POLLEN - 0268-1030-50 - (Aspen)

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Drug Information of POPULUS TREMULOIDES POLLEN

Product NDC: 0268-1030
Proprietary Name: POPULUS TREMULOIDES POLLEN
Non Proprietary Name: Aspen
Active Ingredient(s): .05    g/mL & nbsp;   Aspen
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of POPULUS TREMULOIDES POLLEN

Product NDC: 0268-1030
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of POPULUS TREMULOIDES POLLEN

Package NDC: 0268-1030-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-1030-50)

NDC Information of POPULUS TREMULOIDES POLLEN

NDC Code 0268-1030-50
Proprietary Name POPULUS TREMULOIDES POLLEN
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-1030-50)
Product NDC 0268-1030
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Aspen
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name POPULUS TREMULOIDES POLLEN
Strength Number .05
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 POPULUS TREMULOIDES POLLEN


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