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ULMUS AMERICANA POLLEN - 0268-6708-05 - (American Elm)

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Drug Information of ULMUS AMERICANA POLLEN

Product NDC: 0268-6708
Proprietary Name: ULMUS AMERICANA POLLEN
Non Proprietary Name: American Elm
Active Ingredient(s): 1000    [PNU]/mL & nbsp;   American Elm
Administration Route(s): INTRADERMAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ULMUS AMERICANA POLLEN

Product NDC: 0268-6708
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of ULMUS AMERICANA POLLEN

Package NDC: 0268-6708-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6708-05)

NDC Information of ULMUS AMERICANA POLLEN

NDC Code 0268-6708-05
Proprietary Name ULMUS AMERICANA POLLEN
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6708-05)
Product NDC 0268-6708
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name American Elm
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name ULMUS AMERICANA 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 ULMUS AMERICANA POLLEN


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