Atenolol Tablet Manufacturer in India

WHO-GMP certified manufacturing of Atenolol tablets — 25mg, 50mg and 100mg — a cardioselective beta-blocker for hypertension, angina and arrhythmia management.

Key Highlights

  • WHO-GMP
    Certified

  • Atenolol 25mg
    · 50mg · 100mg Tablet

  • DCGI Approved
    Formulations

  • Contract Manufacturing · 3PM
    · Direct Supply

What We Manufacture

Atenolol Tablet — specifications & clinical context

Product Specifications
Generic Name Atenolol
Strength / Dosage 25mg · 50mg · 100mg
Dosage Form Tablet
Route of Administration Oral
Pack Size Strip of 10 · Bottle of 100
Packaging Alu-PVC blister · Strip packing
Storage Store below 25°C · Protect from moisture
Shelf Life 36 months
Manufacturing Facility  WHO-GMP Certified · Birkoni, Chhattisgarh
Regulatory Status DCGI Approved · Manufacturing Licence Held
Available For Contract manufacturing · Third-party manufacturing · Direct institutional supply
Clinical Context

Atenolol is a first-generation cardioselective beta-blocker — one of the most widely prescribed antihypertensives globally. On the WHO Essential Medicines List. Indicated for hypertension, angina pectoris, cardiac arrhythmias and post-myocardial infarction. The 50mg once-daily dose is the most common antihypertensive regimen. Core government formulary item — high-volume government tender demand in India and across all export markets.

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    Why 9M India

    How Atenolol Tablet is manufactured at 9M India

    • WHO-GMP certified manufacturing process

      Atenolol tablets manufactured through direct compression or wet granulation. Atenolol has good water solubility ensuring rapid and complete dissolution. Moisture barrier packaging required. All three strengths (25mg, 50mg, 100mg) validated at our facility with common manufacturing platform facilitating efficient batch scheduling.

    • In-house QC release testing — every batch

      Dissolution (>80% in 30 min) · Assay by HPLC · Related substances · Content uniformity · Microbial limits — all in-house. COA per batch.

    • Complete documentation within 24 hours

      Manufacturing Licence · DCGI product approvals · WHO-GMP Certificate · Certificate of Analysis · Certificate of Conformance · Stability data (real-time and accelerated, ICH-aligned) — pre-prepared and available within 24 hours for tender submission, export registration or contract manufacturing due diligence.

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    • WHO-GMP
      Certified Facility

    • In-House QC

    • Contract &
      3PM Available

    • DCGI
      Approved

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