Ambrosia artemisiifolia pollen
- Generic Name
- Ambrosia artemisiifolia pollen
- Brand Names
- Ragwitek
- Drug Type
- Biotech
- Unique Ingredient Identifier
- 9W34L2CQ9A
Overview
Ambrosia artemisiifolia pollen is the pollen of the Ambrosia artemisiifolia plant. Ambrosia artemisiifolia pollen is mainly used in allergenic testing.
Background
Ambrosia artemisiifolia pollen is the pollen of the Ambrosia artemisiifolia plant. Ambrosia artemisiifolia pollen is mainly used in allergenic testing.
Indication
Ambrosia artemisiifolia pollen is an allergen extract indicated as immunotherapy for the treatment of short ragweed pollen-induced allergic rhinitis, with or without conjunctivitis, confirmed by positive skin test or in vitro testing for pollen-specific IgE antibodies for short ragweed pollen. It is approved for use in persons five through 65 years of age. This allergen extract is not indicated for the immediate relief of allergic symptoms.
Associated Conditions
- Allergic Rhinitis (AR)
- Allergy to Tree Pollen
- Asthma
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Approved Products
Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
SUBCUTANEOUS, INTRADERMAL | 4000 [AU] in 1 mL | 2011/02/03 | 49288-0837 | ||
SUBCUTANEOUS, INTRADERMAL | 666.667 [AU] in 1 mL | 2010/10/13 | 49288-0793 | ||
SUBCUTANEOUS, INTRADERMAL | 0.0000266 g in 1 mL | 2010/05/06 | 49288-0782 | ||
SUBCUTANEOUS, INTRADERMAL | 0.025 g in 1 mL | 2009/11/13 | 49288-0454 | ||
SUBCUTANEOUS, INTRADERMAL | 0.0125 g in 1 mL | 2009/11/13 | 49288-0431 | ||
SUBCUTANEOUS, INTRADERMAL | 0.0167 g in 1 mL | 2009/11/13 | 49288-0456 | ||
SUBCUTANEOUS, INTRADERMAL | 0.00067 g in 1 mL | 2011/01/13 | 49288-0801 | ||
SUBCUTANEOUS, INTRADERMAL | 20000 [AU] in 1 mL | 2011/12/29 | 49288-0831 | ||
SUBCUTANEOUS, INTRADERMAL | 0.0000266 g in 1 mL | 2010/12/01 | 49288-0799 | ||
SUBCUTANEOUS, INTRADERMAL | 4000 g in 1 mL | 2012/05/11 | 49288-0849 |
EMA Approved Products
Medicine Name | EMA Number | Auth. Holder | Country | Drug Type | Status | Issued | Opinion | Revision |
|---|
No EMA products found
No EMA products found for this drug
HSA Approved Products
Product Name | Manufacturer | Dosage Form | Strength | Approved | Approval No. |
|---|
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 |
|---|
No NMPA products found
No NMPA products found for this drug
PPB Approved Products
Product Name | Registration Code | Company | Category | Sale Type | Reg. Date |
|---|
No PPB products found
No PPB products found for this drug
TGA Approved Products
Product Name | ARTG ID | Sponsor | Status | Reg. Date | Ingredient |
|---|---|---|---|---|---|
32977 | Active | 1991/11/01 | Ambrosia artemisiifolia | ||
351128 | Active | 2020/12/08 | Ambrosia artemisiifolia |