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EUCALYPTUS GLOBULUS POLLEN

NDC 0268-1185 · ALK-Abello, Inc.

Generic nameEucalyptus
Dosage formINJECTION, SOLUTION
RouteSUBCUTANEOUS
Active ingredient(s)EUCALYPTUS GLOBULUS POLLEN
Strength.1 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

0268-1185-50 — 50 mL in 1 VIAL, MULTI-DOSE (0268-1185-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-1186 — Eucalyptus, 0268-6712 — Eucalyptus, 22840-2404 — Eucalyptus globulus, 22840-2405 — Eucalyptus globulus, 22840-4444 — Eucalyptus globulus, 22840-5428 — Eucalyptus globulus, 49643-347 — Eucalyptus globulus, 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, 62713-956 — Allergy Relief, 62713-961 — Allergy Relief, 62713-988 — Echinacea, Baptisia tinctoria, Hydrastis canadensis, Myrrha, Phytolacca decandra, Trigonella foenum-graecum, Zone 9 Tree, Zone 9 Weed, Zone 9 Grass, 62713-989 — Echinacea,Baptisia tinctoria, Hydrastis canadensis, Myrrha, Phytolacca decandra, Trigonella foenum-graecum, Zone 9 Tree, Zone 9 Weed, Zone 9 Grass, 62713-990 — Echinacea, Baptisia tinctoria, Hydrastis canadensis, Myrrha, Phytolacca decandra, Trigonella foenum-graecum, Tropical Tree, Tropical Weed, Tropical Grass, 62713-993 — Allergy Relief, 65044-1564 — Eucalyptus, Eucalyptus globulus, 65044-1565 — Eucalyptus globulus

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