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AMBROSIA TENUIFOLIA POLLEN - 0268-1432-10 - (Ragweed Slender)

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Drug Information of AMBROSIA TENUIFOLIA POLLEN

Product NDC: 0268-1432
Proprietary Name: AMBROSIA TENUIFOLIA POLLEN
Non Proprietary Name: Ragweed Slender
Active Ingredient(s): .05    g/mL & nbsp;   Ragweed Slender
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AMBROSIA TENUIFOLIA POLLEN

Product NDC: 0268-1432
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of AMBROSIA TENUIFOLIA POLLEN

Package NDC: 0268-1432-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-1432-10)

NDC Information of AMBROSIA TENUIFOLIA POLLEN

NDC Code 0268-1432-10
Proprietary Name AMBROSIA TENUIFOLIA POLLEN
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-1432-10)
Product NDC 0268-1432
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Ragweed Slender
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name AMBROSIA TENUIFOLIA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of AMBROSIA TENUIFOLIA POLLEN


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