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PLANTAGO LANCEOLATA POLLEN

NDC 0268-6652 · ALK-Abello, Inc.

Generic nameEnglish Plantain
Dosage formINJECTION, SOLUTION
RoutePERCUTANEOUS
Active ingredient(s)PLANTAGO LANCEOLATA 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

0268-6652-06 — 5 mL in 1 VIAL, MULTI-DOSE (0268-6652-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-1394 — Plantain English, 0268-1395 — Plantain English, 0268-1400 — Plantain English, 0268-8002 — AMARANTHUS RETROFLEXUS POLLEN, CHENOPODIUM ALBUM POLLEN, PLANTAGO LANCEOLATA POLLEN, XANTHIUM STRUMARIUM POLLEN, 0268-8003 — AMARANTHUS RETROFLEXUS POLLEN, CHENOPODIUM ALBUM POLLEN, PLANTAGO LANCEOLATA POLLEN and XANTHIUM STRUMARIUM POLLEN, 0268-8063 — CHENOPODIUM ALBUM POLLEN, IVA ANNUA POLLEN, LANCEOLATA POLLEN and XANTHIUM STRUMARIUM POLLEN, 22840-1365 — Plantago lanceolata, 22840-1366 — Plantago lanceolata, 22840-1367 — Plantago lanceolata, 22840-1368 — Plantago lanceolata, 22840-1370 — Plantago lanceolata, 22840-5321 — Plantago lanceolata, 22840-9309 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9310 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9312 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9313 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9314 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9325 — Plantago lanceolata and Rumex acetosella, 22840-9326 — Plantago lanceolata and Rumex acetosella, 22840-9327 — Plantago lanceolata and Rumex acetosella, +9 more

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