This brand name is authorized in Austria, Australia, Canada, Cyprus, Germany, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Malta, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, United Kingdom, United States, South Africa
The drug LESCOL contains one active pharmaceutical ingredient (API):
1
Fluvastatin
UNII PYF7O1FV7F - FLUVASTATIN SODIUM
|
Fluvastatin, a fully synthetic cholesterol-lowering agent, is a competitive inhibitor of HMG-CoA reductase, which is responsible for the conversion of HMG-CoA to mevalonate, a precursor of sterols, including cholesterol. Fluvastatin reduces total-C, LDL-C, Apo B, and triglycerides, and increases HDL-C in patients with hypercholesterolaemia and mixed dyslipidaemia. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
LESCOL XL Extended-release tablet | FDA, National Drug Code (US) | MPI, US: SPL/PLR |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
C10AA04 | Fluvastatin | C Cardiovascular system → C10 Lipid modifying agents → C10A Lipid modifying agents, plain → C10AA HMG CoA reductase inhibitors |
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): 2863Q, 9236D |
Country: CA | Health Products and Food Branch | Identifier(s): 02250527 |
Country: DE | Bundesinstitut für Arzneimittel und Medizinprodukte | Identifier(s): 13427562, 13987516 |
Country: EE | Ravimiamet | Identifier(s): 1011126, 1060816, 1060827, 1678057, 1678068, 1678079, 1685976, 1685987, 1685998, 1686001, 1686012, 1686023, 1686034, 1686045, 1686056, 1686067, 1686078, 1686089, 1686090, 1686102, 1686113, 1686124, 1686135, 1686146, 1686157, 1686168, 1686179, 1686180, 1686191, 1686203, 1686214, 1686225, 1686595, 1686630, 1723193, 1723205, 1723216, 1723227, 1723238, 1723249, 1723250, 1723261, 1723272, 1723283, 1723294, 1723306, 1723317, 1723328, 1723339, 1723340, 1723351, 1881020, 1881031, 1881042, 1881053, 1881064, 1881075, 1881086, 1881097, 1881109, 1881110, 1881121, 1881165 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 64648 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 011986, 011997 |
Country: FR | Base de données publique des médicaments | Identifier(s): 60852004 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 13881, 147667 |
Country: HR | Agencija za lijekove i medicinske proizvode | Identifier(s): HR-H-337032317 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 39256, 77104 |
Country: IT | Agenzia del Farmaco | Identifier(s): 029163033 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1003486, 1067686, 1068279, 1068280, 1068281, 1068282, 1068283, 1068284, 1068285, 1068286, 1068287, 1068288, 1068289, 1068290, 1068291, 1068292, 1068293, 1068294, 1068295, 1068296, 1091102 |
Country: MT | Medicines Authority | Identifier(s): PI908/00401A |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 59161 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 9691 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100037224, 100037230, 100103056 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W51412001, W51412002, W51412003, W51412004, W51412005, W51412006, W51412007, W51412008, W51412009, W51412010, W51412011, W51412012, W51412013, W51412014, W51412015, W51412016, W51412017, W51412018, W51412019, W51412020, W51412021, W51412022, W51412023, W51412024, W51412025, W51412026 |
Country: SG | Health Sciences Authority | Identifier(s): 11496P |
Country: TN | Direction de la Pharmacie et du Médicament | Identifier(s): 102830231 |
Country: US | FDA, National Drug Code | Identifier(s): 0078-0354 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): 28/7.5/0159, 28/7.5/0160, 35/7.5/0327 |
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