名称
Quercus stellata pollen
描述
Quercus stellata pollen is the pollen of the Quercus stellata plant. Quercus stellata pollen is mainly used in allergenic testing.
种类
Cell-mediated Immunity
Increased Histamine Release
Increased IgG Production
Non-Standardized Pollen Allergenic Extract
同义词
language:english; code:; name;post oak pollen extract
产品
name:3-oak Mix, Black/blackjack/post Pollen
labeller:Allergy Laboratories, Inc.
ndc-id:
ndc-product-code:54575-953
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1967-12-07
ended-marketing-on:
dosage-form:Injection, solution
strength:
route:Percutaneous; Subcutaneous
fda-application-number:BLA101376
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:5-oak Mix, Blackjack/bur/post/red/white Pollen
labeller:Allergy Laboratories, Inc.
ndc-id:
ndc-product-code:54575-954
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1967-12-07
ended-marketing-on:
dosage-form:Injection, solution
strength:
route:Percutaneous; Subcutaneous
fda-application-number:BLA101376
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Allergen Pack Post Oak
labeller:Alvix Laboratories
ndc-id:
ndc-product-code:15455-9014
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:2015-07-20
ended-marketing-on:2018-03-08
dosage-form:Kit
strength:
route:Intradermal; Subcutaneous
fda-application-number:
generic:false
over-the-counter:false
approved:false
country:US
source:FDA NDC
name:Oak Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0331
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-23
ended-marketing-on:
dosage-form:Injection, solution
strength:
route:Intradermal; Subcutaneous
fda-application-number:BLA102223
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Oak Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0332
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-23
ended-marketing-on:
dosage-form:Injection, solution
strength:
route:Intradermal; Subcutaneous
fda-application-number:BLA102223
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Post Oak
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0642
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-23
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102223
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Post Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2489
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.05 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Post Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-4469
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:20000 [PNU]/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Post Oak Pollen
labeller:Allergy Laboratories, Inc.
ndc-id:
ndc-product-code:54575-955
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1967-12-07
ended-marketing-on:
dosage-form:Injection, solution
strength:1 g/20mL
route:Percutaneous; Subcutaneous
fda-application-number:BLA101376
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Post Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-5452
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.025 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
混合物
name:Oak Mixture
ingredients:Quercus alba pollen + Quercus macrocarpa pollen + Quercus muehlenbergii pollen + Quercus palustris pollen + Quercus rubra pollen + Quercus stellata pollen + Quercus velutina pollen + Quercus virginiana pollen
name:Oak Mixture
ingredients:Quercus alba pollen + Quercus macrocarpa pollen + Quercus muehlenbergii pollen + Quercus palustris pollen + Quercus rubra pollen + Quercus stellata pollen + Quercus velutina pollen + Quercus virginiana pollen
name:Post Oak
ingredients:Quercus stellata pollen
name:5-oak Mix, Blackjack/bur/post/red/white Pollen
ingredients:Quercus alba pollen + Quercus macrocarpa pollen + Quercus nigra pollen + Quercus rubra pollen + Quercus stellata pollen
name:3-oak Mix, Black/blackjack/post Pollen
ingredients:Quercus nigra pollen + Quercus stellata pollen + Quercus velutina pollen
name:Post Oak Pollen
ingredients:Quercus stellata pollen
name:Allergen Pack Post Oak
ingredients:Quercus stellata pollen + Sodium chloride
name:Post Oak Pollen
ingredients:Quercus stellata pollen
name:Post Oak Pollen
ingredients:Quercus stellata pollen
name:Post Oak Pollen
ingredients:Quercus stellata pollen
剂量
form:Injection, solution
route:Percutaneous; Subcutaneous
strength:
form:Kit
route:Intradermal; Subcutaneous
strength:
form:Injection, solution
route:Intradermal; Subcutaneous
strength:
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.05 g/1mL
form:Injection, solution
route:Percutaneous; Subcutaneous
strength:1 g/20mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.025 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.05 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:20000 [PNU]/1mL
resource：PubChem Substance
identifier：347910988
resource：RxCUI
identifier：901011