Anthoxanthum odoratum pollen

Overview

Anthoxanthum odoratum pollen is the pollen of the Anthoxanthum odoratum plant. Anthoxanthum odoratum pollen is mainly used in allergenic testing.

Indication

Anthoxanthum odoratum pollen is an allergen extract included in an allergenic testing product called ORALAIR. It is indicated as immunotherapy for the treatment of grass pollen-induced allergic rhinitis with or without conjunctivitis confirmed by positive skin test or in vitro testing for pollen38 specific IgE antibodies for any of the five grass species contained in this product. ORALAIR is approved for use in persons 5 through 65 years of age.

Associated Conditions

Allergic Rhinitis Due to Pollen

Clinical Trials

Title	Posted	Study ID	Phase	Status	Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product	Manufacturer	NDC Code	Route	Strength	Effective Date
Treatment Set TS330317	Antigen Laboratories, Inc.	49288-0684	SUBCUTANEOUS, INTRADERMAL	4000 [BAU] in 1 mL	12/2/2009
Treatment Set TS333938	Antigen Laboratories, Inc.	49288-0657	SUBCUTANEOUS, INTRADERMAL	454.5 [BAU] in 1 mL	12/2/2009
Oralair 100 IR	Stallergenes	59617-0010	SUBLINGUAL	100 [IR] in 1 1	6/9/2025
Treatment Set TS333519	Antigen Laboratories, Inc.	49288-0680	SUBCUTANEOUS, INTRADERMAL	4000 [BAU] in 1 mL	12/2/2009
Treatment Set TS331657	Antigen Laboratories, Inc.	49288-0679	SUBCUTANEOUS, INTRADERMAL	4000 [BAU] in 1 mL	12/2/2009
Oralair 300 IR	Stallergenes	59617-0015	SUBLINGUAL	300 [IR] in 1 1	6/9/2025
Treatment Set TS329123	Antigen Laboratories, Inc.	49288-0688	SUBCUTANEOUS, INTRADERMAL	4000 [BAU] in 1 mL	12/2/2009
Treatment Set TS128811	Antigen Laboratories, Inc.	49288-0675	SUBCUTANEOUS, INTRADERMAL	1428.6 [BAU] in 1 mL	12/2/2009
Treatment Set TS330170	Antigen Laboratories, Inc.	49288-0687	SUBCUTANEOUS, INTRADERMAL	800 [BAU] in 1 mL	12/2/2009
Standardized Sweet Vernal Grass Pollen	Nelco Laboratories, Inc.	36987-2400	SUBCUTANEOUS, INTRADERMAL	10000 [BAU] in 1 mL	11/25/2009

EMA Drug Approvals

Approved Product	Authorization Holder	Status	Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product	Manufacturer	Approval Number	Dosage Form	Strength	Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product	Company	Approval Number	Drug Type	Dosage Form	Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product	Registration No.	Company	Licence No.	Strength	Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product	ARTG ID	Sponsor	Registration Type	Status	Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product	Company	DIN	Dosage Form	Strength	Market Date
ALLERGENIC EXTRACT - STANDARDIZED SWEET VERNAL GRASS POLLEN	alk-abello inc	02325519	Liquid - Subcutaneous , Percutaneous , Intradermal	100000 UNIT / ML	7/30/2009
ALLERGENIC EXTRACT - MIXTURE OF 5 STANDARDIZED GRASS POLLEN	alk-abello inc	02325543	Liquid - Subcutaneous , Percutaneous , Intradermal	20000 UNIT / ML	7/30/2009
ALLERGENIC EXTRACTS - 7 GRASS MIX	greer laboratories inc	02425513	Liquid - Subcutaneous	100000 UNIT / ML	6/2/2014
ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - SWEET VERNAL	greer laboratories inc	02242669	Liquid - Intracutaneous , Subcutaneous	10000 UNIT / ML	2/22/2023
ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - SWEET VERNAL	greer laboratories inc	02242668	Liquid - Subcutaneous , Intracutaneous	100000 UNIT / ML	10/30/2000
ALLERGENIC EXTRACTS - 7 GRASS MIX	greer laboratories inc	02425505	Liquid - Subcutaneous	10000 UNIT / ML	9/25/2014

CIMA AEMPS Drug Approvals

Approved Product	Company	Registration Number	Pharmaceutical Form	Prescription Type	Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product	Company	License Number	Dosage Form	Strength	Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product	Company	License Number	Dosage Form	Strength	Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product	Company	Registration Number	Dosage Form	Strength	Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name	MA Holder	MA Number	Pharmaceutical Form	Active Ingredient	Authorization Date
No UK EMC drug information found for this drug.

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