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Pollens - Trees, Beech, American Fagus grandifolia - 65044-1120-3 - (Beech, American Fagus grandifolia)

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Drug Information of Pollens - Trees, Beech, American Fagus grandifolia

Product NDC: 65044-1120
Proprietary Name: Pollens - Trees, Beech, American Fagus grandifolia
Non Proprietary Name: Beech, American Fagus grandifolia
Active Ingredient(s): .05    g/mL & nbsp;   Beech, American Fagus grandifolia
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Pollens - Trees, Beech, American Fagus grandifolia

Product NDC: 65044-1120
Labeler Name: Jubilant HollisterStier LLC
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103888
Marketing Category: BLA
Start Marketing Date: 19410419

Package Information of Pollens - Trees, Beech, American Fagus grandifolia

Package NDC: 65044-1120-3
Package Description: 30 mL in 1 VIAL (65044-1120-3)

NDC Information of Pollens - Trees, Beech, American Fagus grandifolia

NDC Code 65044-1120-3
Proprietary Name Pollens - Trees, Beech, American Fagus grandifolia
Package Description 30 mL in 1 VIAL (65044-1120-3)
Product NDC 65044-1120
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Beech, American Fagus grandifolia
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19410419
Marketing Category Name BLA
Labeler Name Jubilant HollisterStier LLC
Substance Name FAGUS GRANDIFOLIA 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 Pollens - Trees, Beech, American Fagus grandifolia


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