ID

DB10438||

名称

Neurospora intermedia

描述

Neurospora intermedia is a fungus which can provoke allergic reactions. Neurospora intermedia extract is used in allergenic testing.

cas号

唯一标识码

2072U60DUI

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 Fungal Allergenic Extract

盐类

蛋白质结合

清除

同义词

国际品牌

配送量

产品

name:A Mold Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0004
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1992-04-13
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:A Mold Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0005
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:A Mold Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0006
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:Monilia Mix
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-9642
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Monilia Mix
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-9644
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Monilia Mix
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-9643
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Monilia Mix
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-9677
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Monilia Mix
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-9645
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Monilia Mixture
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0293
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:Neurospora intermedia
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0326
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2011
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2018
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2017
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2016
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2014
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2013
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2015
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2012
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:Neurospora intermedia
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2010
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:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0916
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:40000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0917
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0918
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:0.001 g/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0919
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0920
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:10000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-6538
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:0.10 g/1mL
route:Percutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora Intermedia
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-6539
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:1000 [PNU]/1mL
route:Intradermal
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Neurospora intermedia
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2600
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:Neurospora intermedia
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-5627
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:Neurospora intermedia
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2601
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:Neurospora intermedia
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-1699
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:Neurospora intermedia
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2602
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

混合物

name:A Mold Mixture
ingredients:Aspergillus flavus + Aspergillus fumigatus + Aspergillus niger var. niger + Aspergillus repens + Aureobasidium pullulans var. pullutans + Botrytis cinerea + Candida tropicalis + Chaetomium globosum + Cochliobolus sativus + Epicoccum nigrum + Fusarium oxysporum + Geotrichum candidum + Mucor plumbeus + Mucor racemosus + Neurospora intermedia + Penicillium camemberti + Penicillium chrysogenum var. chrysogenum + Penicillium chrysogenum var. chrysogenum + Penicillium expansum + Penicillium italicum + Penicillium roqueforti + Phoma destructiva + Rhizopus stolonifer + Rhizopus stolonifer + Rhodotorula rubra + Saccharomyces cerevisiae
name:Monilia Mixture
ingredients:Candida tropicalis + Neurospora intermedia
name:A Mold Mixture
ingredients:Aspergillus flavus + Aspergillus fumigatus + Aspergillus niger var. niger + Aspergillus repens + Aureobasidium pullulans var. pullutans + Botrytis cinerea + Candida tropicalis + Chaetomium globosum + Cochliobolus sativus + Epicoccum nigrum + Fusarium oxysporum + Geotrichum candidum + Mucor plumbeus + Mucor racemosus + Neurospora intermedia + Penicillium camemberti + Penicillium chrysogenum var. chrysogenum + Penicillium chrysogenum var. chrysogenum + Penicillium expansum + Penicillium italicum + Penicillium roqueforti + Phoma destructiva + Rhizopus stolonifer + Rhizopus stolonifer + Rhodotorula rubra + Saccharomyces cerevisiae
name:A Mold Mixture
ingredients:Aspergillus flavus + Aspergillus fumigatus + Aspergillus niger var. niger + Aspergillus repens + Aureobasidium pullulans var. pullutans + Botrytis cinerea + Candida tropicalis + Chaetomium globosum + Cochliobolus sativus + Epicoccum nigrum + Fusarium oxysporum + Geotrichum candidum + Mucor plumbeus + Mucor racemosus + Neurospora intermedia + Penicillium camemberti + Penicillium chrysogenum var. chrysogenum + Penicillium chrysogenum var. chrysogenum + Penicillium expansum + Penicillium italicum + Penicillium roqueforti + Phoma destructiva + Rhizopus stolonifer + Rhizopus stolonifer + Rhodotorula rubra + Saccharomyces cerevisiae
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Neurospora Intermedia
ingredients:Neurospora intermedia
name:Monilia Mix
ingredients:Candida albicans + Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Monilia Mix
ingredients:Candida albicans + Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Neurospora intermedia
ingredients:Neurospora intermedia
name:Monilia Mix
ingredients:Candida albicans + Neurospora intermedia
name:Monilia Mix
ingredients:Candida albicans + Neurospora intermedia
name:Monilia Mix
ingredients:Candida albicans + Neurospora intermedia

包装者

生产者

价格

受影响的生物体

剂量

form:Injection, solution
route:Intradermal; Subcutaneous
strength:
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:
form:Injection, solution
route:Intradermal
strength:1000 [PNU]/1mL
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:Injection, solution
route:Percutaneous
strength:0.10 g/1mL
form:Injection, solution
route:Subcutaneous
strength:0.001 g/1mL
form:Injection, solution
route:Subcutaneous
strength:10000 [PNU]/1mL
form:Injection, solution
route:Subcutaneous
strength:20000 [PNU]/1mL
form:Injection, solution
route: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：347910607
resource：RxCUI
identifier：867274

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