Box Elder - 49288-0059-3 - (Box Elder)

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Drug Information of Box Elder

Product NDC: 49288-0059
Proprietary Name: Box Elder
Non Proprietary Name: Box Elder
Active Ingredient(s): .1    g/mL & nbsp;   Box Elder
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Box Elder

Product NDC: 49288-0059
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Box Elder

Package NDC: 49288-0059-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0059-3)

NDC Information of Box Elder

NDC Code 49288-0059-3
Proprietary Name Box Elder
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0059-3)
Product NDC 49288-0059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Box Elder
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ACER NEGUNDO 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 Box Elder


General Information