VIMOVO

This brand name is authorized in Austria, Brazil, Canada, Estonia, Spain, Finland, Ireland, Lithuania, Netherlands, Romania, United Kingdom, United States, South Africa

Active ingredients

The drug VIMOVO contains a combination of these active pharmaceutical ingredients (APIs):

1 Naproxen
UNII 57Y76R9ATQ - NAPROXEN

Naproxen is a non-steroidal anti-inflammatory analgesic compound with antipyretic properties as has been demonstrated in classical animal test systems. Naproxen exhibits its anti-inflammatory effect even in adrenalectomised animals, indicating that its action is not mediated through the pituitary-adrenal axis.

Read about Naproxen
2 Esomeprazole
UNII R6DXU4WAY9 - ESOMEPRAZOLE MAGNESIUM

Esomeprazole is the S-isomer of omeprazole and reduces gastric acid secretion through a specific targeted mechanism of action. Esomeprazole is a weak base and is concentrated and converted to the active form in the highly acidic environment of the secretory canaliculi of the parietal cell, where it inhibits the enzyme H+ K+ -ATPase – the acid pump and inhibits both basal and stimulated acid secretion.

Read about Esomeprazole

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
VIMOVO Delayed release tablet FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
M01AE52 Naproxen and esomeprazole M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AE Propionic acid derivatives
Discover more medicines within M01AE52

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 542820040006917, 542820040007017
Country: CA Health Products and Food Branch Identifier(s): 02361701, 02361728
Country: EE Ravimiamet Identifier(s): 1437768, 1437779, 1437780, 1437791, 1437803, 1437814, 1437825, 1460179
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 73182
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 431530
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 182339
Country: IE Health Products Regulatory Authority Identifier(s): 23216
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1050688, 1050916, 1058591, 1058592, 1058593, 1058594, 1058595, 1058596, 1058597, 1058598, 1058599, 1058600, 1089161
Country: NL Z-Index G-Standaard, PRK Identifier(s): 95710
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68965001, W68965002, W68965003, W68965004, W68965005, W68965006, W68965007, W68965008, W68965009, W68965010, W68965011, W68965012, W68965013, W68965014, W68965015, W68965016, W68965017, W68965018, W68965019, W68965020, W68965021, W68965022, W68965023, W68965024, W68965025, W68965026, W68965027, W68965028, W68965029, W68965030, W68965031, W68965032, W68965033, W68965034
Country: US FDA, National Drug Code Identifier(s): 75987-030, 75987-031
Country: ZA Health Products Regulatory Authority Identifier(s): 45/3.1/0179

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