HK Neopharm Limited is one of the most reliable manufacturers and suppliers of vortioxetine hydrobromide tablets in China, featured by quality products and good price. Please rest assured to buy vortioxetine hydrobromide tablets in stock here and get quotation from our factory. Customized orders are welcome.
Vortioxetine Hydrobromide Tablets are a new-generation multi-target 5‑hydroxytryptamine modulator oral antidepressant with dual effects of antidepressant and cognitive improvement. With mild adverse reactions, good tolerability and low impact on sexual function, it is a first-line preferred drug for acute, maintenance and continuation treatment of adult depression, widely used in psychiatric clinical practice, and consistently recommended by authoritative guidelines at home and abroad.
Technical Specifications
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Product Name |
Vortioxetine Hydrobromide Tablets |
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Synonyms |
Vortioxetine Hydrobromide Oral Tablets, Vortioxetine Hydrobromide Drug Tablets |
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Characteristics |
5 mg: Pink, almond-shaped film-coated tablets 10 mg: Yellow, almond-shaped film-coated tablets |
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CAS Number |
960203-27-4 |
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Assay |
≥99.0% (HPLC, Subject to the COA) |
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Formula |
C₁₈H₂₂N₂S·HBr |
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Package |
Technical Package |
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Storage |
Store at ＜30℃ |
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Structure |
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Product Features
Multi-target mechanism, dual effects of antidepressant and cognitive improvemen. tThrough 5‑HT reuptake inhibition + 5‑HT₁A agonism + 5‑HT₁B partial agonism + 5‑HT₃/5‑HT₇ antagonism, it rapidly improves depression, anhedonia, anxiety and sleep disorders, and significantly improves attention, memory and executive function, especially suitable for depressive patients with cognitive impairment.
Definite efficacy and excellent Vortioxetine Hydrobromide Tablets: 10mg once daily can take effect rapidly. The most common adverse reaction is nausea, mostly mild to moderate and transient in the first two weeks of treatment, generally not affecting drug withdrawal. The impact on sexual function is significantly lower than traditional SSRI/SNRI, with higher long-term treatment compliance.
Convenient administration and flexible dosage. Oral administration, with or without food. The initial and recommended dose for adults is 10 mg/day, which can be adjusted to 5 mg–20 mg/day according to efficacy and tolerability. No gradual tapering is required for drug withdrawal, making clinical use convenient.
Wide applicable population and friendly to special populations. For the treatment of adult depression. The recommended initial dose for elderly patients is 5 mg. No dosage adjustment is required in patients with mild to moderate hepatic/renal impairment, with wide application range and large individualization space.
Recommended by authoritative guidelines with sufficient evidence-based medicine. Recommended by guidelines of China, the United States, Europe and other countries for acute and maintenance treatment of adult major depressive disorder (MDD), with sufficient evidence-based evidence and clear clinical status.
Full-Cycle Quality Control & Consistent Quality
This product implements the highest quality control standards for oral solid preparations, with closed-loop control from raw materials, granulation, tableting, coating to finished product release:
Strict raw material control: Only Vortioxetine Hydrobromide meeting ICH and pharmacopoeia standards is used, and full inspection is required before use.
Prescription and process: Optimize excipient ratio and granulation process to ensure uniform dissolution, accurate content, strong stability, no discoloration, no delamination and no degradation during long-term storage.
Full inspection before release: Each batch is issued with a complete COA, covering traits, identification, related substances, isomers, content, dissolution rate, uniformity, microbial limit and other indicators, with traceable data and excellent batch-to-batch consistency.
Stability verification: Valid for 48 months after stress testing, accelerated and long-term storage inspection, with stable and reliable quality during the storage period.
Application Scenarios
Acute treatment of adult depression. Rapidly improve core depressive symptoms, relieve depression, anhedonia, anxiety, sleep disorders, and improve social function and quality of life.
Maintenance and continuation treatment. Continuous treatment for ≥6 months after symptom relief to consolidate efficacy and significantly reduce the risk of recurrence, suitable for patients with recurrent and chronic depression.
Depression with cognitive impairment. For patients with depression accompanied by decreased attention, memory loss and impaired executive function, achieve simultaneous improvement of mood and cognition.
Replacement for poor efficacy/intolerance of traditional antidepressants. For patients with insufficient efficacy of SSRI/SNRI, or those who need to switch drugs due to obvious sexual dysfunction and adverse reactions.
Research and registration. For generic drug consistency evaluation, prescription process development, BE test, registration declaration, providing stable reference preparations and complete compliant data.
Packaging and Transportation
Light and moisture-proof packaging
Aluminum-plastic blister + sealed carton, light-proof, moisture-proof and anti-oxidation to ensure stability within the validity period.
Room temperature storage and transportation
Transport at ＜30℃ in a cool and dry place, no cold chain required, avoid high temperature, direct sunlight exposure and humid environment.
Compliant logistics
GSP qualified pharmaceutical logistics, full traceability; complete customs declaration and documents for international transportation, global compliant delivery.
Validity period management
First-in first-out, regular sampling inspection, validity period early warning to ensure clinical and research use within the validity period.
Our Advantages
Mature prescription and process, stable quality. Adopting international mainstream prescription and coating technology, with consistent dissolution, accurate content and extremely low impurities, in line with ChP, USP, EP standards, meeting the requirements of consistency evaluation.
Complete specifications, clinical adaptation. Provide Vortioxetine Hydrobromide Tablets 5 mg/10 mg/20 mg full specifications, covering the full dose requirements of initial, adjustment and maintenance, suitable for different populations and treatment stages.
Stable supply and reliable delivery time. Large-scale production capacity and sufficient spot stock, quickly respond to orders from hospitals, pharmaceutical enterprises and research institutions to ensure long-term continuous supply.
Complete compliant documents and technical support. Provide complete documents including COA, MSDS, GMP certificate, stability data, dissolution curve, supporting registration declaration and hospital access.
Excellent tolerability and compliance. Mild adverse reactions, low impact on sexual function, convenient administration, significantly improve the long-term treatment completion rate of patients and reduce the recurrence rate.
FAQ
The company always takes product quality and clinical drug safety as the core principle, specializing in supplying high-purity and stable-quality Vortioxetine Hydrobromide Tablets, the whole production process is in line with international GMP and pharmacopoeia standards, and the whole process is traceable. From drug research and development, prescription verification to commercial supply, we can provide sustained and stable product support for various projects. We look forward to sincere cooperation with customers around the world to contribute to the innovation and development of psychiatric and depression treatment with high-quality preparations, and build a long-term, trusted and win-win stable cooperative relationship.
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