SOLU-CORTEF

This brand name is authorized in Australia, Canada, Estonia, Finland, Hong Kong, Croatia, Ireland, Israel, Japan, Malta, Netherlands, New Zealand, Singapore, United Kingdom, United States, South Africa

Active ingredients

The drug SOLU-CORTEF contains one active pharmaceutical ingredient (API):

1 Hydrocortisone
UNII 50LQB69S1Z - HYDROCORTISONE SODIUM SUCCINATE

Hydrocortisone is the main glucocorticoid secreted by the adrenal cortex. Hydrocortisone is an anti-inflammatory steroid. Its anti-inflammatory action is due to reduction in the vascular component of the inflammatory response and reduction in the formation of inflammatory fluid and cellular exudates.

Read about Hydrocortisone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
Solu-Cortef 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
H02AB09 Hydrocortisone H Systemic hormonal preparations, excl. Sex hormones and insulins → H02 Corticosteroids for systemic use → H02A CORTICOSTEROIDS FOR SYSTEMIC USE, PLAIN → H02AB Glucocorticoids
Discover more medicines within H02AB09

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 1501B, 1510L, 1511M, 3096Y, 3470P, 3471Q, 5118J, 5119K
Country: CA Health Products and Food Branch Identifier(s): 00030600, 00030619, 00030627, 00030635
Country: EE Ravimiamet Identifier(s): 1009066
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 439954, 496943, 523273
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 138713, 41828
Country: HK Department of Health Drug Office Identifier(s): 00471, 25551
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-226141869
Country: IE Health Products Regulatory Authority Identifier(s): 46612
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8129, 8219
Country: JP 医薬品医療機器総合機構 Identifier(s): 2452400D3052, 2452400D6060, 2452400D7040
Country: MT Medicines Authority Identifier(s): AA565/67101
Country: NL Z-Index G-Standaard Identifier(s): 14043912
Country: NL Z-Index G-Standaard, PRK Identifier(s): 20400
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 1672
Country: SG Health Sciences Authority Identifier(s): 04791P
Country: US FDA, National Drug Code Identifier(s): 0009-0005, 0009-0011, 0009-0013, 0009-0016, 0009-0825, 51662-1261, 51662-1262, 55154-3942
Country: ZA Health Products Regulatory Authority Identifier(s): G/21.5/201

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.