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Red Oak Pollen

NDC 22840-2491 · Greer Laboratories, Inc.

Generic nameQuercus rubra
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)QUERCUS RUBRA POLLEN
Strength10000 [PNU]/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

22840-2491-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-2491-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-1319 — Oak Red, 0268-6642 — Red Oak, 0268-8000 — ACER NEGUNDO POLLEN, BETULA NIGRA POLLEN, BLACK WALNUT, CARYA OVATA POLLEN, FRAXINUS AMERICANA POLLEN, PLATANUS OCCIDENTALIS POLLEN, POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN, QUERCUS RUBRA POLLEN, SALIX NIGRA POLLEN and ULMUS AMERICANA POLLEN, 0268-8070 — QUERCUS RUBRA, QUERCUS ALBA, QUERCUS VIRGINIANA, 22840-2490 — Quercus rubra, 22840-2492 — Quercus rubra, 22840-2493 — Quercus rubra, 22840-2494 — Quercus rubra, 22840-2495 — Quercus rubra, 22840-5453 — Quercus rubra, 22840-9441 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9442 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9443 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9444 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9445 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9447 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9448 — Fagus grandifolia, Populus deltoides, Quercus rubra, Betula nigra, Carya ovata and Fraxinus americana, 22840-9449 — Fagus grandifolia, Populus deltoides, Quercus rubra, Betula nigra, Carya ovata and Fraxinus americana, 22840-9450 — Fagus grandifolia, Populus deltoides, Quercus rubra, Betula nigra, Carya ovata and Fraxinus americana, 22840-9452 — Fagus grandifolia, Populus deltoides, Quercus rubra, Betula nigra, Carya ovata and Fraxinus americana, +55 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.