ID

DB10740||

名称

Quercus gambelii pollen

描述

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

cas号

唯一标识码

9HC15X34LX

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;Gambels oak pollen extract

国际品牌

配送量

产品

name:Arizona Gambel Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-4460
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:Arizona Gambel Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-5447
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:Arizona Gambel Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2479
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:Arizona Gambel Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2481
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:Arizona Gambel Oak Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2480
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:Gambel Oak
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0356
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:Gambels Oak Pollen
labeller:Allermed Laboratories, Inc.
ndc-id:
ndc-product-code:49643-404
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-12
ended-marketing-on:
dosage-form:Injection
strength:0.05 g/1mL
route:Cutaneous; Intradermal; Subcutaneous
fda-application-number:BLA102211
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2855
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2859
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2857
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2860
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2853
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2858
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2854
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:Gambil Oak
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2856
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

混合物

name:Gambel Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambil Oak
ingredients:Quercus gambelii pollen
name:Gambels Oak Pollen
ingredients:Quercus gambelii pollen
name:Arizona Gambel Oak Pollen
ingredients:Quercus gambelii pollen
name:Arizona Gambel Oak Pollen
ingredients:Quercus gambelii pollen
name:Arizona Gambel Oak Pollen
ingredients:Quercus gambelii pollen
name:Arizona Gambel Oak Pollen
ingredients:Quercus gambelii pollen
name:Arizona Gambel Oak Pollen
ingredients:Quercus gambelii pollen

包装者

生产者

价格

受影响的生物体

剂量

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:40000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.05 g/1mL
form:Injection
route:Cutaneous; 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

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：347910869
resource：RxCUI
identifier：852276

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