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Beech pollen - Prescription Drug Labeling

Product NDC Code 49643-349
Drug Name

Beech pollen

Type Brand
Pharm Class Non-Standardized Pollen Allergenic Extract [EPC],
Increased Histamine Release [PE],
Cell-mediated Immunity [PE],
Increased IgG Production [PE],
Pollen [CS],
Allergens [CS]
Active Ingredients
Fagus grandifolia pollen .05 g/ml
Application Number BLA102211
Labeler Name Allermed Laboratories, Inc.
Package NDC Code Description
49643-349-05 5 ml in 1 vial, multi-dose (49643-349-05)
49643-349-10 10 ml in 1 vial, multi-dose (49643-349-10)
49643-349-30 30 ml in 1 vial, multi-dose (49643-349-30)
49643-349-50 50 ml in 1 vial, multi-dose (49643-349-50)

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