NEO-MEDROL

This brand name is authorized in Nigeria.

Active ingredients

The drug NEO-MEDROL contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 43502P7F0P - METHYLPREDNISOLONE ACETATE
 

Methylprednisolone is a synthetic glucocorticoid and a methyl derivative of prednisolone. Methylprednisolone is a potent anti-inflammatory agent with the capacity to profoundly inhibit the immune system.

 
Read more about Methylprednisolone
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 407PSC3OC7 - ALUMINUM CHLOROHYDRATE ANHYDROUS
 

Aluminium chloride hexahydrate acts locally, in the stratum comeum and in the terminal duct, to relieve hyperhidrosis. It is is acidic and is thought to act by diffusing into the sweat ducts where on neutralisation it forms gelatinous hydroxides which obstruct the flow of sweat.

 
Read more about Aluminium chloride
4
UNII 70FD1KFU70 - SULFUR
 
Read more about Sulfur

Medicine classification

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

ATC Group Classification
D07CA02 Methylprednisolone and antibiotics D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07C Corticosteroids, combinations with antibiotics → D07CA Corticosteroids, weak, combinations with antibiotics
Discover more medicines within D07CA02

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 04-3778
Switch country to Nigeria in order to find specific presentations of NEO-MEDROL

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