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At IndiGlobal Exports, we’re more than just a pharmaceutical export company—we’re a purpose-driven mission to make high-quality Indian healthcare products accessible worldwide.Founded in Panchkula, Haryana, we exist to bridge India’s pharmaceutical i...

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Tenofovir Disoproxil Fumarate Tablets IP 300 mg

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Accept Small Orders: No

Country Of Origin : India

Tenofovir Disoproxil Fumarate Tablets IP 300 mg is a pharmaceutical product indicated for supplements treatment. This formulation is manufactured with export-quality standards to ensure therapeutic efficacy, consistent dosage, and compliance with international healthcare regulations.

Features:
  • Used in the management of supplements conditions
  • Precise dosage form and active pharmaceutical ingredients
  • Suitable for international pharmaceutical markets
  • Manufactured in GMP-compliant facilities
  • Reliable therapeutic performance
Attributes:
  • Category: Supplements
  • Formulation: Tablet
  • Packaging: Export-grade blister or strip packs
  • Shelf Life: As per regulatory standards
  • Manufacturer: IndiGlobal Exports

  • Additional Information

    Product Overview

    Tenofovir Disoproxil Fumarate Tablets IP 300 mg is developed for the effective management of supplements conditions, offering reliable performance backed by stringent pharmaceutical standards. Each batch is carefully produced and tested to ensure consistency, safety, and compliance with global export norms.


    Therapeutic Use & Application

    This formulation supports the clinical treatment and ongoing care of patients with supplements indications. Commonly prescribed in hospital and retail pharmacy settings, it ensures measurable therapeutic benefit.


    Formulation & Packaging

    Crafted in state-of-the-art facilities, this tablet formulation ensures accuracy in dosing and ease of administration. It is typically available in secure blister or strip packs suitable for bulk export or institutional supply.


    Quality & Compliance

    The product is manufactured in facilities adhering to WHO-GMP standards and complies with pharmacopoeial quality benchmarks (IP/USP). Ideal for regulated and semi-regulated markets seeking quality-assured medications.

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