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American Beech - 49288-0073-1 - (American Beech)

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Drug Information of American Beech

Product NDC: 49288-0073
Proprietary Name: American Beech
Non Proprietary Name: American Beech
Active Ingredient(s): .05    g/mL & nbsp;   American Beech
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Beech

Product NDC: 49288-0073
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of American Beech

Package NDC: 49288-0073-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0073-1)

NDC Information of American Beech

NDC Code 49288-0073-1
Proprietary Name American Beech
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0073-1)
Product NDC 49288-0073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name American Beech
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name FAGUS GRANDIFOLIA POLLEN
Strength Number .05
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 Beech


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