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VENLASIGN XR Capsule by BluepillExpress, under the Dr Precision label, is a high-quality extended-release antidepressant formulation containing Venlafaxine Hydrochloride. Designed for the treatment of major depressive disorder (MDD), generalized anxiety disorder (GAD), panic disorder, and social anxiety disorder, this capsule ensures steady plasma drug levels and sustained symptom relief through advanced extended-release technology such as polymer matrix or SODAS. The unique dual mechanism of action as a serotonin-norepinephrine reuptake inhibitor (SNRI) addresses complex mood and anxiety disorders, especially in patients who do not respond well to SSRIs. Manufactured under stringent GMP standards with pharmaceutical-grade excipients, VENLASIGN XR provides enhanced patient compliance with once-daily dosing and minimizes peak-related side effects including nausea and dizziness. The tamper-proof, moisture-resistant packaging is optimized for hot and humid climates and supports global distribution. Available in various strengths from 37.5 mg to 150 mg and beyond, VENLASIGN XR facilitates dose titration and safer discontinuation profiles, also being utilized off-label for chronic pain and neuropathy. The product is backed by comprehensive clinical data, compliant regulatory documentation including Certificates of Analysis, and customized packaging and branding options, making it a reliable choice for healthcare professionals and pharmaceutical distributors seeking precision, efficacy, and regulatory compliance in extended-release antidepressant formulations.
Key Features
| Features | Description |
|---|---|
| Active Ingredient | Venlafaxine Hydrochloride |
| Formulation Type | Extended-Release Capsule |
| Indications | Major Depressive Disorder, Generalized Anxiety Disorder, Panic Disorder, Social Anxiety Disorder |
| Mechanism of Action | Serotonin-Norepinephrine Reuptake Inhibitor (SNRI) with dose-dependent dual neurotransmitter modulation |
| Release Technology | Polymer matrix or SODAS for controlled 24-hour drug release |
| Dosage Strengths | 37.5 mg to 150 mg and higher |
| Quality Standards | Manufactured under GMP-compliant conditions following WHO, ISO, and FDA standards |
| Packaging | Tamper-proof, moisture-resistant with alu-alu blister, HDPE containers, or custom packaging |
| Special Features | Minimized peak side effects, improved patient compliance with once-daily dosing, reduced withdrawal symptoms |
| Support | Includes Certificate of Analysis, bioequivalence data, stability profiles, and regulatory documents |
| Attributes | Description |
|---|---|
| Manufacturer | BluepillExpress |
| Brand | Dr Precision |
| Pharmaceutical Form | Extended-Release Capsule |
| Therapeutic Class | Antidepressant (SNRI) |
| Indications | MDD, GAD, Panic Disorder, Social Anxiety Disorder |
| Active Substance Concentration | 37.5 mg to 150 mg Venlafaxine HCl per capsule |
| Release Mechanism | Advanced polymer matrix or SODAS technology for 24-hour consistent release |
| Packaging Options | Alu-Alu blister packs, HDPE containers, customized formats |
| Storage Conditions | Suitable for hot and humid climates; moisture-resistant packaging |
| Regulatory Compliance | WHO-GMP, ISO, local FDA equivalence |
| Safety Profile | Requires blood pressure monitoring at higher doses; contraindicated with MAOIs; caution in cardiovascular, hepatic, seizure disorders |
| Clinical Support | Bioequivalence and stability data, regulatory documentation, private label/custom branding available |
*Disclaimer: The above description has been AI-generated and has not been audited or verified for accuracy. It is recommended to verify product details independently before making any purchasing decisions.
VENLASIGN XR uses advanced polymer matrix or spheroidal oral drug absorption systems (SODAS) to provide a controlled 24-hour release of Venlafaxine Hydrochloride, thereby maintaining steady plasma concentrations and minimizing peak-related side effects.
The extended-release formulation of VENLASIGN XR minimizes peak plasma concentration spikes, which substantially reduces side effects such as nausea and dizziness commonly experienced with immediate-release Venlafaxine.
Yes, VENLASIGN XR is also used off-label in certain patient populations to manage chronic pain syndromes, menopausal hot flashes, and diabetic neuropathy due to its SNRI mechanism.
BluepillExpress manufactures VENLASIGN XR under GMP-compliant conditions, with rigorous in-process controls, validated techniques, pharmaceutical-grade excipients, and adheres to WHO-GMP, ISO, and local FDA-equivalent standards, providing Certificates of Analysis with each batch.
VENLASIGN XR is available in tamper-proof, moisture-resistant alu-alu blister packs, HDPE containers, and can also be customized with customer-specified packaging formats suitable for hot and humid climates and regulatory compliance in various markets.
Careful dose titration with VENLASIGN XR helps optimize therapeutic outcomes while reducing the risk of side effects and withdrawal symptoms. The extended-release design further supports a safer discontinuation process.
VENLASIGN XR should not be used in pediatric populations without strict physician supervision due to safety considerations and lack of established pediatric dosing.
Country Of Origin: India
VENLASIGN XR Capsule is an extended-release antidepressant formulation containing Venlafaxine Hydrochloride, manufactured by BluepillExpress. It is used in the treatment of major depressive disorder (MDD), generalized anxiety disorder (GAD), panic disorder, and social anxiety disorder. This extended-release formulation ensures steady plasma levels, enhanced compliance, and sustained relief from mood-related symptoms.
This product is manufactured under the Dr Precision label, ensuring GMP-compliant quality and precision formulation standards.
VENLASIGN XR Capsule is a meticulously engineered pharmaceutical product from BluepillExpress that delivers Venlafaxine Hydrochloride in an extended-release format for long-lasting therapeutic action. Venlafaxine is a serotonin-norepinephrine reuptake inhibitor (SNRI), a class of antidepressants known for their dual mechanism in modulating both serotonin and norepinephrine neurotransmitters in the brain. This dual-action profile offers robust efficacy in treating a spectrum of affective and anxiety-related disorders, especially in patients unresponsive to SSRIs.
VENLASIGN XR is primarily indicated for major depressive disorder, generalized anxiety disorder, social anxiety disorder, and panic disorder. The extended-release capsule is designed using advanced polymer matrix or spheroidal oral drug absorption systems (SODAS) that gradually release the active ingredient over 24 hours, thereby maintaining consistent drug levels in plasma. This pharmacokinetic advantage minimizes peak-related side effects such as nausea and dizziness, and helps maintain symptom control with once-daily dosing.
The formulation of VENLASIGN XR by BluepillExpress is compliant with international GMP protocols, incorporating rigorous in-process controls, validated manufacturing techniques, and pharmaceutical-grade excipients to ensure the highest standard of efficacy, safety, and shelf-stability. The capsules are tamper-proof, moisture-resistant, and optimized for global distribution, suitable for hot and humid climates due to their enhanced packaging systems.
Venlafaxine’s mechanism involves the inhibition of the reuptake of serotonin at lower doses, with norepinephrine reuptake inhibition becoming more prominent at higher doses. This dose-dependent dual mechanism is beneficial in treatment-resistant depression and anxiety. The extended-release form also reduces the incidence of withdrawal symptoms during tapering, offering a safer and more tolerable discontinuation profile. VENLASIGN XR is available in strengths ranging from 37.5 mg to 150 mg or higher, depending on the therapeutic requirements and physician guidance.
Therapeutically, patients on VENLASIGN XR often begin to experience improvements in sleep, mood, concentration, and energy within 1–2 weeks of therapy, with full therapeutic effect evident within 4–6 weeks. Clinicians often use it as a second-line or augmentative treatment when SSRI monotherapy is ineffective. It is also used off-label for chronic pain syndromes, menopausal hot flashes, and diabetic neuropathy in select patient populations.
VENLASIGN XR requires careful dose titration and should be taken consistently with food to improve gastrointestinal tolerability. BluepillExpress provides full support for clinical use, including data on bioequivalence, stability profiles, and international labeling compliance. Each production batch is accompanied by a Certificate of Analysis and regulatory documents necessary for product registration in both regulated and semi-regulated markets.
Safety considerations include monitoring for elevated blood pressure at higher doses, risk of serotonin syndrome when combined with other serotonergic agents, and discontinuation syndrome if the medication is stopped abruptly. VENLASIGN XR is contraindicated in patients with hypersensitivity to venlafaxine or those on monoamine oxidase inhibitors (MAOIs). Caution is advised in patients with cardiovascular conditions, seizure disorders, and hepatic impairment. It should not be used in pediatric populations without physician supervision.
BluepillExpress ensures that VENLASIGN XR Capsules are manufactured in facilities accredited by global regulatory authorities, including WHO-GMP, ISO, and local FDA equivalents. Packaging options are available in alu-alu blister packs, HDPE containers, or customer-specified formats to meet country-specific guidelines and market needs. Custom branding and private label services are also available for clients seeking differentiation in competitive mental health markets.
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