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American beech pollen - Prescription Drug Labeling

Product NDC Code 22840-4434
Drug Name

American beech pollen

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Increased IgG Production [PE],
Non-Standardized Pollen Allergenic Extract [EPC],
Pollen [CS]
Active Ingredients
Fagus grandifolia pollen .1 g/ml
Route INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Dosage Form SOLUTION
Application Number BLA101833
Labeler Name Greer Laboratories, Inc.
Packages
Package NDC Code Description
22840-4434-2 10 ml in 1 vial, multi-dose (22840-4434-2)

Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API