Skip to main content

Gray (White) Birch Pollen

NDC 49643-325 · Allermed Laboratories, Inc.

Generic nameBetula populifolia
Dosage formINJECTION
RouteCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active ingredient(s)BETULA POPULIFOLIA 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

49643-325-05 — 5 mL in 1 VIAL, MULTI-DOSE (49643-325-05)

49643-325-10 — 10 mL in 1 VIAL, MULTI-DOSE (49643-325-10)

49643-325-30 — 30 mL in 1 VIAL, MULTI-DOSE (49643-325-30)

49643-325-50 — 50 mL in 1 VIAL, MULTI-DOSE (49643-325-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-8024 — BETULA NIGRA, BETULA POPULIFOLIA, 22840-1457 — Betula populifolia, 22840-1458 — Betula populifolia, 22840-1459 — Betula populifolia, 22840-1460 — Betula populifolia, 22840-1461 — Betula populifolia, 22840-1462 — Betula populifolia, 22840-5415 — Betula populifolia, 22840-9403 — Betula lenta, Betula nigra and Betula populifolia, 22840-9404 — Betula lenta, Betula nigra and Betula populifolia, 22840-9405 — Betula lenta, Betula nigra and Betula populifolia, 22840-9407 — Betula lenta, Betula nigra and Betula populifolia, 22840-9408 — Betula lenta, Betula nigra and Betula populifolia, 22840-9493 — Betula lenta, Betula nigra and Betula populifolia

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