Truflav-500 Tablet
Diosmin 450 mg + Hesperidin 50 mg Tablets
| Composition | Diosmin 450 mg + Hesperidin 50 mg |
|---|---|
| Dosage Form | Tablet |
| Pack Type | Alu-Alu Blister |
| Pack Size | 10 x 10 Tablets |
| MRP | ₹ 2490 |
| Therapy | Vascular / Surgery — Venotonic Flavonoid |
| Storage | Store below 30 °C in a dry place, protected from light and moisture. |
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About Truflav-500 Tablet
Truflav-500 Tablet provides Diosmin 450 mg + Hesperidin 50 mg — venotonic for chronic venous insufficiency, varicose veins, post-haemorrhoidectomy support.
Manufactured by Trumac Healthcare under WHO-GMP.
Indications
- Chronic venous insufficiency
- Varicose veins
- Haemorrhoids (acute and chronic)
- Lymphoedema (mild)
Mechanism of Action
Diosmin is a flavonoid that improves venous tone and capillary fragility — for chronic venous insufficiency, varicose veins, haemorrhoids. Hesperidin is co-flavonoid enhancing absorption.
Dosage & Administration
Adults: 1 tablet twice daily.
Side Effects
Generally well tolerated. Mild GI upset, headache.
Contraindications & Precautions
Hypersensitivity, pregnancy first trimester.
Storage
Store below 30 °C in a dry place, protected from light and moisture.
Truflav-500 Tablet is available for monopoly-based PCD pharma franchise across India and for third-party manufacturing under your brand. WHO-GMP certified, with full visual-aid and promotional support. Become a Trumac franchise partner →
Frequently Asked Questions
What is Truflav-500 Tablet used for?
Truflav-500 Tablet contains Diosmin 450 mg + Hesperidin 50 mg. Used as per the indications described above.
How should Truflav-500 Tablet be taken?
As directed by your physician. Complete the prescribed course.
Is Truflav-500 Tablet available for PCD pharma franchise?
Yes, Trumac Healthcare offers Truflav-500 Tablet on monopoly-based PCD pharma franchise and for third-party manufacturing.
How should Truflav-500 Tablet be stored?
Store below 30 °C in a dry place, protected from light and moisture.
Is Truflav-500 Tablet WHO-GMP certified?
Yes, manufactured in WHO-GMP and DCGI-compliant facilities.
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