Anthoxanthum odoratum pollen
- Generic Name
- Anthoxanthum odoratum pollen
- Brand Names
- Oralair 100, Oralair 300, Oralair Children and Adolescents Sample Kit
- Drug Type
- Biotech
- Unique Ingredient Identifier
- 2KIK19R45Y
Overview
Anthoxanthum odoratum pollen is the pollen of the Anthoxanthum odoratum plant. Anthoxanthum odoratum pollen is mainly used in allergenic testing.
Background
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 |
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No clinical trials found
No clinical trials found for this drug
FDA Approved Products
Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
SUBCUTANEOUS, INTRADERMAL | 10000 [BAU] in 1 mL | 2009/11/25 | 36987-2400 | ||
SUBCUTANEOUS, INTRADERMAL | 100000 [BAU] in 1 mL | 2009/11/25 | 36987-2399 | ||
PERCUTANEOUS, SUBCUTANEOUS | 100000 [BAU] in 1 mL | 2010/03/27 | 54575-106 | ||
SUBCUTANEOUS, INTRADERMAL | 4000 [BAU] in 1 mL | 2009/12/02 | 49288-0682 | ||
SUBCUTANEOUS, INTRADERMAL | 4000 [BAU] in 1 mL | 2009/12/02 | 49288-0679 | ||
SUBCUTANEOUS, INTRADERMAL | 1428.6 [BAU] in 1 mL | 2009/12/02 | 49288-0675 | ||
SUBCUTANEOUS, INTRADERMAL | 800 [BAU] in 1 mL | 2009/12/02 | 49288-0687 | ||
SUBCUTANEOUS, INTRADERMAL | 454.5 [BAU] in 1 mL | 2009/12/02 | 49288-0657 | ||
SUBCUTANEOUS, INTRADERMAL | 4000 [BAU] in 1 mL | 2009/12/02 | 49288-0680 | ||
SUBCUTANEOUS, INTRADERMAL | 4000 [BAU] in 1 mL | 2009/12/02 | 49288-0688 |
EMA Approved Products
Medicine Name | EMA Number | Auth. Holder | Country | Drug Type | Status | Issued | Opinion | Revision |
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No EMA products found
No EMA products found for this drug
HSA Approved Products
Product Name | Manufacturer | Dosage Form | Strength | Approved | Approval No. |
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No HSA products found
No HSA products found for this drug
NMPA Approved Products
Product Name | Approval No. | Manufacturer | Dosage Form | Trade Name | Strength | Type | Status | Date | Import |
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No NMPA products found
No NMPA products found for this drug
PPB Approved Products
Product Name | Registration Code | Company | Category | Sale Type | Reg. Date |
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No PPB products found
No PPB products found for this drug
TGA Approved Products
Product Name | ARTG ID | Sponsor | Status | Reg. Date | Ingredient |
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No TGA products found
No TGA products found for this drug