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R K D Pharmaceutical LLP is a globally focused pharmaceutical export and healthcare sourcing company providing access to high-quality pharmaceutical formulations, APIs, excipients, nutraceuticals, medical devices, surgical consumables, laboratory ins...

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Aceclofenac 100mg & Paracetamol 500mg Tablets

SKU: AC03
Price upon request
  • Product is not available

SKU: AC03

Country of origin : India

Active Strength & Dosage Form

Aceclofenac 100mg & Paracetamol 500mg Tablets are fixed-dose oral tablets containing 100 mg of aceclofenac and 500 mg of paracetamol per unit. The combination brings together aceclofenac, a non-steroidal anti-inflammatory drug, and paracetamol, an analgesic and antipyretic ingredient. Pharmaceutical distributors and institutional procurement teams should verify the dosage-form specification, batch certificate of analysis (COA), prescription classification and destination-market authorization before purchasing.

Composition & Product Characteristics

Each tablet contains aceclofenac 100 mg and paracetamol 500 mg together with formulation-specific excipients used to support manufacturing and tablet performance. Finished-product assessment should cover identification and assay of both active ingredients, related substances, dissolution, disintegration, uniformity of dosage units, microbial quality and packaging integrity. Tablet coating, appearance, excipient composition, storage conditions and pack configuration should be confirmed through the manufacturer’s approved specification and technical documentation.

  • Additional Information

    Formulation Application & Compatibility

    Aceclofenac 100mg & Paracetamol 500mg Tablets is part of our Pharmaceutical Products range for pharmaceutical distributors, wholesalers and institutional procurement teams. Each oral tablet contains aceclofenac 100 mg and paracetamol 500 mg in a fixed-dose combination intended for approved pain-management applications. Buyers should match the offered dosage form, pharmacopoeial specifications, excipient profile, packaging and labelling with the registration, distribution and tender requirements of the destination market. As a prescription pharmaceutical product in many markets, it must be supplied and used according to approved labelling and qualified healthcare guidance.

    • Country of Origin: Confirm from the manufacturer or supplier
    • Regulatory/Pharmacopoeial Compliance: Confirm the applicable BP, IP or destination-market standards and finished-product authorization from supporting documents
    • Quality Assurance / Shelf Life: Confirm batch-release testing, approved storage conditions and labelled shelf life from the COA and manufacturer documentation

    Manufacturing Compliance & Documentation

    Request an Aceclofenac 100 mg & Paracetamol 500 mg Tablets Procurement Quote

    Frequently Asked Questions

    • What are the minimum order quantities and bulk order options for Aceclofenac 100 mg & Paracetamol 500 mg Tablets? Minimum order quantities depend on the manufacturer, pack configuration, destination market and regulatory requirements. Buyers should share their expected volume, preferred pack size and supply schedule to confirm available options.
    • How is pricing structured for large-volume purchases? Pricing may vary according to order quantity, packaging format, documentation requirements, destination and agreed shipment terms. Provide the required quantity, pack configuration and Incoterm to obtain a suitable commercial quotation.
    • Are COA and pharmacopoeial documents available for this product? Documentation availability must be verified before ordering. Buyers may request the batch COA, finished-product specification, manufacturing authorization, stability information and documents required for registration, tendering or import clearance.
    • What logistics and lead-time considerations apply to shipments? Lead time depends on manufacturing availability, batch-release testing, packaging, documentation and destination-country import procedures. Storage and transportation must follow the conditions stated in the approved product documentation.
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