Overview
Anthoxanthum odoratum allergenic extract is used in allergenic testing.
Indication
Anthoxanthum odoratum 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 |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
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 |
|---|---|---|---|---|---|
| SOUTHERN GRASS MIX (1:20) Scratch test & treatment | 32705 | Medicine | A | 11/1/1991 | |
| ALUSTAL POLLEN EXTRACT OF FIVE GRASSES MAINTENANCE 10 IR/mL injection suspension vial | 132847 | Medicine | A | 10/3/2006 | |
| GRASS MIX #7 (1:20) Scratch test & treatment | 32714 | Medicine | A | 11/1/1991 | |
| ORALAIR Continuation Treatment Sublingual (Allergen pollen Extract of 5 grasses) Tablets 300IR blister pack | 167566 | Medicine | A | 5/3/2011 | |
| ALUSTAL POLLEN EXTRACT OF FIVE GRASSES INITIAL TREATMENT injection suspension vial composite pack | 132848 | Medicine | A | 10/3/2006 | |
| ORALAIR Initiation Treatment, Sublingual (Allergen pollen Extract of 5 grasses) Tablets 100IR & 300IR Blister Pack | 167565 | Medicine | A | 5/3/2011 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| STANDARDIZED GRASS POLLEN - SWEET VERNALGRASS | hollister-stier laboratories llc | 02238496 | Liquid - Intradermal | 100 UNIT / ML | N/A |
| HOMEOPATHIC MEDICINE (S NO. 304) DPS 30C | total health centre | 02076462 | Drops - Oral | 30 C / ML | 12/31/1994 |
| STANDARDIZED GRASS POLLEN - SWEET VERNAL GRASS (10,000 BAU/ML) | 02238494 | Solution - Percutaneous
,
Subcutaneous | 10000 UNIT / ML | 4/11/2001 | |
| PACIFIC GRASSES & WEED POLLEN VACCINE | bencard allergy laboratories, an allergy therapeutics (canada) ltd. company | 00061441 | Liquid - Subcutaneous | null NIL / NIL | 12/31/1955 |
| STANDARDIZED GRASS POLLEN - SWEET VERNALGRASS | hollister-stier laboratories llc | 02238495 | Liquid - Intradermal | 1000 UNIT / ML | N/A |
| STANDARDIZED GRASS POLLEN - SWEET VERNAL GRASS (100,000 BAU/ML) | 02238493 | Solution - Percutaneous
,
Subcutaneous | 100000 UNIT / ML | 10/18/2000 |
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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