Overview
No overview information available.
Indication
⑴作乳化剂和稳定剂:用本品制备的乳剂,乳粒小,一般在1μm以下,吸收率高,物理性质稳定,不宜分层,可热压蒸汽灭菌。 ⑵作增溶剂:本品可因表面活性剂形成胶团,增加多种难溶性药物的表观溶解度。 ⑶作吸收促进剂:一方面由于本品使肠蠕动变慢,药物在胃肠道滞留时间增长,吸收增加,从而提高口服制剂的生物利用度。另一方面,本品与皮肤相容性佳,增加皮肤通透性,可促进外用药剂的吸收。 ⑷作固体分散的载体:固体型号的产品可作为一些固体分散物的载体(如灰黄霉素、地高辛、洋地黄毒苷等)从而大大地提高这些药物的溶解度,促进这些药物的吸收。用量一般在2%~10%。 ⑸作乳膏剂、栓剂基质:固体型号的本品,可作基质使用,起到缓释与延效的作用。 ⑹作缓释材料:分子量大的固体产品,用作黏合剂、包衣材料,可使制剂达到缓释、控释的目的。用量5%~15%。
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2005/06/03 | Phase 2 | Completed |
FDA Drug Approvals
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No FDA approvals found for this drug. |
EMA Drug Approvals
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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COLOXYL INFANT DROPS poloxamer 100mg/mL oral liquid bottle (reformulation) | 124463 | Medicine | A | 12/21/2005 |
Health Canada Drug Approvals
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No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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