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American Elm Pollen - 49643-417-10 - (Ulmus americana)

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Drug Information of American Elm Pollen

Product NDC: 49643-417
Proprietary Name: American Elm Pollen
Non Proprietary Name: Ulmus americana
Active Ingredient(s): 1    g/20mL & nbsp;   Ulmus americana
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Elm Pollen

Product NDC: 49643-417
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of American Elm Pollen

Package NDC: 49643-417-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-417-10)

NDC Information of American Elm Pollen

NDC Code 49643-417-10
Proprietary Name American Elm Pollen
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-417-10)
Product NDC 49643-417
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Ulmus americana
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name ULMUS AMERICANA POLLEN
Strength Number 1
Strength Unit g/20mL
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 American Elm Pollen


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