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PINUS ECHINATA POLLEN

NDC 0268-6748 · ALK-Abello, Inc.

Generic nameYellow Pine
Dosage formINJECTION, SOLUTION
RoutePERCUTANEOUS
Active ingredient(s)PINUS ECHINATA 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

0268-6748-06 — 5 mL in 1 VIAL, MULTI-DOSE (0268-6748-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-1390 — Pine Yellow, 22840-3465 — Pinus echinata, 22840-3466 — Pinus echinata, 22840-3467 — Pinus echinata, 22840-5467 — Pinus echinata, 22840-9434 — Pinus taeda, Pinus strobus and Pinus echinata, 22840-9435 — Pinus taeda, Pinus strobus and Pinus echinata, 22840-9436 — Pinus taeda, Pinus strobus and Pinus echinata, 22840-9437 — Pinus taeda, Pinus strobus and Pinus echinata, 22840-9439 — Pinus taeda, Pinus strobus and Pinus echinata, 22840-9440 — Pinus taeda, Pinus strobus and Pinus echinata, 49643-448 — Pinus echinata, 49643-524 — Pinus echinata/Pinus ponderosa/Pinus strobus, 58264-0304 — JUNIPERUS ASHEI POLLEN, JUNIPERUS VIRGINIANA POLLEN, TAMARIX GALLICA POLLEN, CUPRESSUS ARIZONICA POLLEN, TAXODIUM DISTICHUM POLLEN, JUNIPERUS MONOSPERMA POLLEN, JUNIPERUS PINCHOTII POLLEN, JUNIPERUS SCOPULORUM POLLEN, PINUS TAEDA POLLEN, PINUS STROBUS POLLEN, and PINUS ECHINATA POLLEN, 58809-213 — Antigens All Zones Grasses Trees and Weeds. Baptisia tinctoria, Echinacea, Hydrastis canadensis, Myrrha, Nasturtium aquaticum, Phytolacca decandra, Urtica urens, 58809-214 — Antigens All Zones Grasses Trees and Weeds. Baptisia tinctoria, Echinacea, Hydrastis canadensis, Myrrha, Nasturtium aquaticum, Phytolacca decandra, Urtica urens, 58809-215 — Antigens All Zones Grasses, Trees, and Weeds. Baptisia tinctoria, Echinacea, Hydrastis canadensis, Myrrha, Nasturtium aquaticum, Phytolacca decandra, Urtica urens

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