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Amoxicillin 500mg Capsules

Broad-spectrum penicillin antibiotic — WHO-GMP approved and available across 35+ markets worldwide.

Capsule Antibiotic Elite Division Active

Amoxicillin 500mg

Generic Name: Amoxicillin Trihydrate

Strength: 500 mg  ·  Pack Size: 10 capsules × 10 blisters / box

Amoxicillin 500mg is a broad-spectrum semi-synthetic penicillin antibiotic manufactured under WHO-GMP conditions at Laborate's Panipat facility. It is indicated for the treatment of susceptible bacterial infections of the respiratory tract, urinary tract, skin and soft tissue. Registered and supplied across Africa, CIS, MENA and South-East Asia.

Product Specifications

Generic Name
Amoxicillin Trihydrate
Therapeutic Area
Anti-infective
Dosage Form
Hard Gelatin Capsule
Strength
500 mg
Route of Administration
Oral
Pack Size
10 capsules × 10 blisters / box — 100 capsules / box
Storage
Store below 25°C in a cool, dry place. Protect from light and moisture.
Shelf Life
36 months from date of manufacture
Division
Elite Division
Prescription Status
Schedule H (Prescription Only Medicine)
Regulatory Status
Active — WHO-GMP Approved
Available Markets
India, Sub-Saharan Africa, CIS, MENA, South-East Asia
Export Availability
Yes — registered and supplied to Africa, CIS and MENA via Exports Division
HS Code
3004.10.10

Product Description

Pharmacological Action

Amoxicillin is a semi-synthetic, broad-spectrum penicillin antibiotic. It exerts its bactericidal action by inhibiting the biosynthesis of bacterial cell wall peptidoglycan, making it effective against a wide range of Gram-positive and selected Gram-negative organisms.

Indications

Amoxicillin 500mg Capsules are indicated for the treatment of:

  • Acute bacterial infections of the upper and lower respiratory tract (including community-acquired pneumonia and acute exacerbation of chronic bronchitis)
  • Uncomplicated urinary tract infections caused by susceptible organisms
  • Skin and soft tissue infections
  • Dental and oral infections
  • Typhoid fever and other Salmonella infections (where susceptibility is confirmed)

Dosage & Administration

Adults and children over 40 kg: 250–500 mg every 8 hours or 750 mg–1 g every 12 hours (depending on severity). Treatment course typically 5–10 days. Always follow prescriber directions and local antimicrobial stewardship guidelines.

Manufacturing Standards

Manufactured at Laborate’s Panipat facility under WHO-GMP conditions using API sourced from audited, GMP-certified suppliers. Each batch undergoes rigorous in-process quality control and finished-product testing against British Pharmacopoeia (BP) and Indian Pharmacopoeia (IP) standards before release.

Contraindications & Precautions

Contraindicated in patients with known hypersensitivity to penicillins or any component of the formulation. Cross-reactivity with cephalosporins may occur in sensitive patients. Use with caution in renal impairment; dosage adjustment may be required. Not recommended in infectious mononucleosis (risk of rash).

Downloads

Technical documents and regulatory dossiers available on request.

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