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Ivermectin Tablets product packshot

Ivermectin Tablets

Composition: Ivermectin BP 3 mg; Ivermectin IP 6 mg (uncoated)

Usage: Treatment of selected parasitic infections as prescribed

Category: Antiparasitic / Anthelmintic

Therapeutic category: Antiparasitic agent

SKU: Ivermectin Tablets

Categories: Pharmaceutical Exporter India, Pharmaceutical Formulations India, WHO GMP Certified Formulations

Product Information

Ivermectin Tablets is listed in our pharmaceutical product portfolio for business-to-business enquiries. Product-specific formulation details, available strengths, dosage form, pack configuration and supply terms should be confirmed against the current product specification before ordering.

For distributor, wholesaler, hospital procurement and export enquiries, please request the applicable product specifications, batch documentation, shelf-life information, packaging options and regulatory documents. Availability and documentation depend on the product and destination market.

Description

1. Product Introduction

Healthy Life Pharma Pvt. Ltd. presents Ivermectin Tablets for antiparasitic treatment. Ivermectin is an anthelmintic medicine used for certain infections caused by parasitic worms. Use for other parasitic conditions, including scabies or public-health programs, depends on local approvals and clinical guidance.

Manufacturer: Healthy Life Pharma Pvt. Ltd.   Exporter: Healthy Inc. Contract manufacturing and export arrangements are subject to confirmation of product approvals, available capacity and destination-country requirements.

2. Product Specifications

Product nameIvermectin Tablets
Composition – BPEach tablet contains Ivermectin BP 3 mg
Composition – IPEach uncoated tablet contains Ivermectin IP 6 mg
Strengths confirmed by supplied labels3 mg and 6 mg
Other strength12 mg mentioned in marketing description; availability and approved composition not confirmed
CAS number70288-86-7
Therapeutic classAnthelmintic / antiparasitic (not an antibiotic)
Dosage formOral tablets; 6 mg specified as uncoated
Packaging / shelf lifeConfirm against approved product label and stability data
SKUIvermectin Tablets

3. Manufacturing Technology

Ivermectin has limited water solubility, making particle properties, blend uniformity, tablet disintegration and dissolution important formulation considerations. Suitable manufacturing methods may include controlled blending, granulation and compression, depending on the validated product formula. Specific claims about micronization, solid dispersions or dispersible pediatric versions require product-level confirmation.

4. Quality Assurance

Relevant quality controls may include identity, assay, related substances, content uniformity, dissolution and stability testing against the applicable approved pharmacopoeial or registered specification. Ivermectin contains closely related homologues; applicable composition requirements should be verified for the selected standard. Batch certificates and manufacturing authorizations should be confirmed before commercial publication.

5. Pharmacology and Clinical Use

Ivermectin acts primarily on glutamate-gated chloride channels in susceptible invertebrates, disrupting neuromuscular function and leading to paralysis of parasites. Clinical indications depend on the product's local authorization and treatment guidelines.

  • Intestinal strongyloidiasis: An established indication for certain oral ivermectin products.
  • Onchocerciasis: Reduces microfilarial burden; retreatment may be necessary.
  • Scabies: Oral treatment may be used under relevant clinical guidance, depending on jurisdiction and patient factors.
  • Lymphatic filariasis: May be included in specific supervised mass drug administration programs.

Ivermectin is not an antibacterial antibiotic and is not an approved treatment for viral infections such as COVID-19.

6. Export and Regulatory Support

For prospective B2B partners, documentation may include a certificate of analysis, product specifications, stability data and registration dossiers where available. FSC, COPP, GMP documents and CTD/ACTD submissions must be verified for the actual manufacturing site, product and destination country. Shipment terms and packaging options are quotation-dependent.

7. Frequently Asked Questions

Q: What strengths are listed?
A: Ivermectin BP 3 mg and Ivermectin IP 6 mg are specified in the supplied product labels. A 12 mg variant is mentioned separately but not substantiated by a composition statement.

Q: Is ivermectin an antibiotic?
A: No. It is an antiparasitic/anthelmintic medicine.

Q: Is it taken as a single dose?
A: Treatment schedules vary by infection, body weight, local guidance and patient circumstances; some conditions require repeat treatment.

Q: Is it suitable for every patient?
A: No. Pregnancy, young children, interacting medicines and certain co-infections require individualized clinical assessment.

8. Dosage and Administration

Use only according to the prescribing clinician and the approved local label. Oral ivermectin dosing is typically weight-based and varies by condition. Strongyloidiasis, onchocerciasis and scabies use different protocols and retreatment intervals. Administration with or without food must follow the particular product label and indication; do not assume a universal regimen. Never substitute veterinary ivermectin formulations for human medicines.

9. Side Effects and Precautions

  • Possible adverse effects include nausea, diarrhea, dizziness, itching and rash.
  • Patients treated for onchocerciasis can experience inflammatory Mazzotti-type reactions due to dying microfilariae.
  • Loa loa co-infection: Patients with high microfilarial loads may face serious neurologic complications; assess epidemiologic risk before treatment.
  • Seek urgent medical care for severe allergic reactions, altered consciousness, seizures or other serious symptoms.
  • Pregnancy, breastfeeding, pediatric use and medicine interactions require professional assessment.

10. Storage Instructions

Store in the original packaging, protected from moisture and light as stated on the approved product label. The supplied description suggests storage below 30°C, but the final storage conditions must match the registered product. Keep out of reach of children.