POLYDEX-N

This brand name is authorized in Nigeria.

Active ingredients

The drug POLYDEX-N contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 7S5I7G3JQL - DEXAMETHASONE
 

Dexamethasone is a synthetic glucocorticoid; it combines high anti-inflammatory effects with low mineralocorticoid activity. It has an approximately 7 times greater anti-inflammatory potency than prednisolone, another commonly prescribed corticosteroid. At high doses it reduces the immune response.

 
Read more about Dexamethasone
2
UNII 057Y626693 - NEOMYCIN SULFATE
 

Neomycin is an aminoglycoside antibiotic and acts by binding to polysomes, inhibiting protein synthesis and generating errors in the transcription of the genetic code.

 
Read more about Neomycin
3
UNII 19371312D4 - POLYMYXIN B SULFATE
 

Polymixin B is bactericidal against a wide range of gram negative bacilli. It exerts a bactericidal effect by binding to acid phospholipids in the cell wall and membranes of the bacterium, thereby rendering ineffective the osmotic barrier normally provided by the cell membrane.

 
Read more about Polymyxin B

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
B4-1717 Suspension/Drops Polydex-N Eye Drops SUSP_DROPS 0.1%; 0.35%; 6000 IU/mL 5 mL (in plastic dropper bottle) Ophthalmic Suspension Each mL contains: Dexamethasone 0.1%, Neomycin Sulphate 3,500 I.U., Polymyxin B Sulphate 6,000 I.U. 28/10/2021

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
S01CA01 Dexamethasone and antiinfectives S Sensory organs → S01 Ophthalmologicals → S01C Antiinflammatory agents and antiinfectives in combination → S01CA Corticosteroids and antiinfectives in combination
Discover more medicines within S01CA01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
NG Registered Drug Product Database B4-1717

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