Home > National Drug Code (NDC) > Beech Pollen

Beech Pollen - 49643-349-10 - (Fagus grandifolia)

Alphabetical Index


Drug Information of Beech Pollen

Product NDC: 49643-349
Proprietary Name: Beech Pollen
Non Proprietary Name: Fagus grandifolia
Active Ingredient(s): 1    g/20mL & nbsp;   Fagus grandifolia
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Beech Pollen

Product NDC: 49643-349
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Beech Pollen

Package NDC: 49643-349-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-349-10)

NDC Information of Beech Pollen

NDC Code 49643-349-10
Proprietary Name Beech Pollen
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-349-10)
Product NDC 49643-349
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Fagus grandifolia
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name FAGUS GRANDIFOLIA 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 Beech Pollen


General Information