This brand name is authorized in Cyprus, Ireland, Malta, United Kingdom
The drug SOLU-MEDRONE contains one active pharmaceutical ingredient (API):
1
Methylprednisolone
UNII LEC9GKY20K - METHYLPREDNISOLONE SODIUM SUCCINATE
|
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. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
SOLU-MEDRONE Powder for injection | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
H02AB04 | Methylprednisolone | H Systemic hormonal preparations, excl. Sex hormones and insulins → H02 Corticosteroids for systemic use → H02A CORTICOSTEROIDS FOR SYSTEMIC USE, PLAIN → H02AB Glucocorticoids |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 41795, 41804, 43925, 43931 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 46671, 46701 |
Country: MT | Medicines Authority | Identifier(s): AA565/39901, AA565/39902 |
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