ID

DB10742||

名称

Quercus nigra pollen

描述

Quercus nigra pollen is the pollen of the Quercus nigra plant. Quercus nigra pollen is mainly used in allergenic testing.

cas号

唯一标识码

6U600U1326

状态

组

approved,

指示

药效学

作用机制

毒性

代谢

吸收

半衰期

分类

消除途径

种类

Cell-mediated Immunity

Increased Histamine Release

Increased IgG Production

Non-Standardized Pollen Allergenic Extract

盐类

蛋白质结合

清除

同义词

language:english; code:; name;water oak pollen extract

国际品牌

配送量

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:Blackjack Oak Pollen
labeller:Allergy Laboratories, Inc.
ndc-id:
ndc-product-code:54575-949
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:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2888
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2887
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2891
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2889
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:40000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2892
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.1 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2885
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:10000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2890
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2886
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:10000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-3403
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.1 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-3404
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:40000 [PNU]/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-3405
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.001 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Water Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-4418
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:Water Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-5455
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

混合物

name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Water Oak
ingredients:Quercus nigra pollen
name:Blackjack Oak Pollen
ingredients:Quercus nigra 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:Water Oak Pollen
ingredients:Quercus nigra pollen
name:Water Oak Pollen
ingredients:Quercus nigra pollen
name:Water Oak Pollen
ingredients:Quercus nigra pollen
name:Water Oak Pollen
ingredients:Quercus nigra pollen
name:Water Oak Pollen
ingredients:Quercus nigra pollen

包装者

生产者

价格

受影响的生物体

剂量

form:Injection, solution
route:Percutaneous; Subcutaneous
strength:
form:Injection, solution
route:Percutaneous; Subcutaneous
strength:1 g/20mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.05 g/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.1 g/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:10000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:20000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:40000 [PNU]/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.001 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.05 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.1 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:20000 [PNU]/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:40000 [PNU]/1mL

atc代码

fda标签

化学品安全技术说明书

专利

食物相互作用

药物相互作用

序列

实验性质

外部标识符

resource：PubChem Substance
identifier：347910871
resource：RxCUI
identifier：1013944

外部链接

路径

目标

酶

载体

运输工具

药物反应

效应

不良反应