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American Elm - 49288-0190-1 - (American Elm)

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Drug Information of American Elm

Product NDC: 49288-0190
Proprietary Name: American Elm
Non Proprietary Name: American Elm
Active Ingredient(s): .1    g/mL & nbsp;   American Elm
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Elm

Product NDC: 49288-0190
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of American Elm

Package NDC: 49288-0190-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0190-1)

NDC Information of American Elm

NDC Code 49288-0190-1
Proprietary Name American Elm
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0190-1)
Product NDC 49288-0190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name American Elm
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ULMUS AMERICANA POLLEN
Strength Number .1
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 American Elm


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