MEDROL

This brand name is authorized in United States. It is also authorized in Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Israel, Italy, Japan, Lithuania, New Zealand, Poland, Romania, Tunisia.

Active ingredients

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

1	Methylprednisolone UNII X4W7ZR7023 - METHYLPREDNISOLONE
	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

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
MEDROL Tablet	MPI, US: SPL/Old	FDA, National Drug Code (US)

Medicine classification

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

ATC Group		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
Discover more medicines within H02AB04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
CA	Health Products and Food Branch	00030988, 00036129
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	28897-06-09, 28898-06-09
EE	Ravimiamet	1009077, 1009099, 1065754, 1738324, 1738335, 1866922, 1868328
FI	Lääkealan turvallisuus- ja kehittämiskeskus	111245, 117729, 139082, 159103, 174284, 453125
FR	Base de données publique des médicaments	60224316, 60988157, 64639548
HR	Agencija za lijekove i medicinske proizvode	HR-H-123990428, HR-H-251851390, HR-H-371675611
IL	מִשְׂרַד הַבְּרִיאוּת	84
IT	Agenzia del Farmaco	014159040
JP	医薬品医療機器総合機構	2456003F1034, 2456003F2030
LT	Valstybinė vaistų kontrolės tarnyba	1001231, 1001232, 1001233, 1058666, 1058667, 1066055, 1078904
NZ	Medicines and Medical Devices Safety Authority	4919, 4920
PL	Rejestru Produktów Leczniczych	100042308, 100042314
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W65155001, W65156001, W65157001
TN	Direction de la Pharmacie et du Médicament	6530052, 6530053
US	FDA, National Drug Code	0009-0020, 0009-0022, 0009-0056, 0009-0073, 0009-0176, 50090-0092