LOTEMAX

This brand name is authorized in Austria, Canada, Cyprus, Estonia, Hong Kong, Ireland, Israel, Lithuania, Poland, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa

Active ingredients

The drug LOTEMAX contains one active pharmaceutical ingredient (API):

1 Loteprednol
UNII YEH1EZ96K6 - LOTEPREDNOL ETABONATE

Loteprednol etabonate is a new class of corticosteroid with potent antiinflammatory activity designed to be active at the site of action. Its antiinflammatory activity is similar to the most powerful steroid used in ophthalmology but with less intraocular pressure.

Read about Loteprednol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
LOTEMAX Eye-drops, suspension Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
S01BA14 Loteprednol S Sensory organs → S01 Ophthalmologicals → S01B Antiinflammatory agents → S01BA Corticosteroids, plain
Discover more medicines within S01BA14

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02321114, 02421941, 02435853
Country: EE Ravimiamet Identifier(s): 1185184, 1185195, 1185207
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 134647
Country: HK Department of Health Drug Office Identifier(s): 51822
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 6453, 8187
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1019880, 1019881, 1019882
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100158382, 100419960
Country: SG Health Sciences Authority Identifier(s): 12601P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 24063011
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8681738340013, 8681738440034, 8699856710038
Country: US FDA, National Drug Code Identifier(s): 24208-299, 24208-443, 24208-503, 24208-507
Country: ZA Health Products Regulatory Authority Identifier(s): 37/15.2/0588

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