ULTRACORTENOL

This brand name is authorized in Austria, Cyprus, Estonia, Finland, Croatia, Malta, Netherlands, Romania

Active ingredients

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

1 Prednisolone UNII 24W6S37NXU - PREDNISOLONE PIVALATE

Prednisolone is a glucocorticoid which has anti-inflammatory activity. Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs are primarily used for their potent anti-inflammatory effects in disorders of many organ systems. Read about Prednisolone

Medicine classification

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

ATC code	Group title	Classification
S01BA04	Prednisolone	S Sensory organs → S01 Ophthalmologicals → S01B Antiinflammatory agents → S01BA Corticosteroids, plain
Discover more medicines within S01BA04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EE	Ravimiamet	Identifier(s): 1821484
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 485006
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-169337333
Country: MT	Medicines Authority	Identifier(s): MA1276/00201
Country: NL	Z-Index G-Standaard	Identifier(s): 12154881
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 7919
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W67470001