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American Sycamore - 49288-0485-5 - (American Sycamore)

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Drug Information of American Sycamore

Product NDC: 49288-0485
Proprietary Name: American Sycamore
Non Proprietary Name: American Sycamore
Active Ingredient(s): .1    g/mL & nbsp;   American Sycamore
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Sycamore

Product NDC: 49288-0485
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 Sycamore

Package NDC: 49288-0485-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0485-5)

NDC Information of American Sycamore

NDC Code 49288-0485-5
Proprietary Name American Sycamore
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0485-5)
Product NDC 49288-0485
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name American Sycamore
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PLATANUS OCCIDENTALIS 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 Sycamore


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