Zithrum-250

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Zithrum-250

Zithrum-250 Tablet contains Azithromycin, a macrolide antibiotic used for the treatment of various bacterial infections. It works by inhibiting bacterial protein synthesis, thereby preventing the growth and spread of susceptible bacteria. Azithromycin is known for its broad-spectrum activity and convenient dosing schedule.

Each uncoated tablet contains:

  • Azithromycin Dihydrate I.P.
      Equivalent to Anhydrous Azithromycin — 250 mg
  • Excipients: q.s.
  • Colour: Titanium Dioxide I.P.
  • Upper and lower respiratory tract infections

  • Ear, nose & throat (ENT) infections

  • Skin and soft tissue infections

  • Community-acquired pneumonia

  • Sexually transmitted infections (as prescribed)

  • Other infections caused by Azithromycin-sensitive organisms

  • As directed by the physician.

Medicine Production Process

01

Research & Development (R&D)

New drug molecules are discovered, tested, and optimized for safety, efficacy, and stability.

02

Pre-Formulation Studies

Understanding the drug’s physical, chemical, and biological properties to design the right dosage form.

03

Formulation Development

Creating the final dosage form (tablet, capsule, injection, etc.) with excipients to ensure effectiveness.

04

Raw Material Procurement

High-quality active pharmaceutical ingredients (APIs) and excipients are sourced under strict compliance.

05

Weighing & Dispensing

Precise measurement of raw materials to maintain consistency and quality in every batch.

06

Granulation / Mixing

APIs and excipients are blended or granulated to achieve uniformity for tablet or capsule production.

07

Compression / Filling

The mixture is compressed into tablets or filled into capsules with accuracy.

08

Coating / Finishing

Tablets may be coated for taste masking, controlled release, or product stability.

09

Sterilization (for Injectables)

Parenteral products undergo sterilization to ensure they are safe and free from contaminants.

10

Quality Control (QC) Testing

Each batch is rigorously tested for purity, potency, safety, and compliance with regulatory standards.

11

Packaging

Medicines are packed in blisters, bottles, or sachets with labeling and batch details for traceability.

12

Storage & Distribution

Finished products are stored under controlled conditions and distributed through the pharma supply chain.