American Beech Pollen
NDC 22840-5410 · Greer Laboratories, Inc.
Generic nameFagus grandifolia
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)FAGUS GRANDIFOLIA POLLEN
Strength.05 g/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]
Marketing categoryBLA
Packages
22840-5410-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-5410-2)
22840-5410-4 — 50 mL in 1 VIAL, MULTI-DOSE (22840-5410-4)
22840-5410-5 — 5 mL in 1 BOTTLE, DROPPER (22840-5410-5)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0268-1046 — Beech, 0268-1047 — Beech, 0268-6607 — Beech, 22840-1437 — Fagus grandifolia, 22840-4434 — Fagus grandifolia, 49643-349 — Fagus grandifolia, 65044-1120 — Beech, American Fagus grandifolia, 65044-1121 — Beech, American Fagus grandifolia