MedPath

Poloxamer

Generic Name
Poloxamer

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.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
COLOXYL INFANT DROPS poloxamer 100mg/mL oral liquid bottle (reformulation)
124463
Medicine
A
12/21/2005

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.