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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Paracetamol Tablets 500mg
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Product is not available
Country of origin : India
Active Strength & Dosage Form
Paracetamol Tablets 500mg are oral solid-dose products containing 500 mg of paracetamol in each tablet. Paracetamol is an analgesic and antipyretic active ingredient used for the symptomatic relief of pain and fever. Pharmaceutical distributors and institutional buyers should verify the dosage-form specification, applicable pharmacopoeial standard, batch certificate of analysis (COA) and destination-market authorization before procurement.
Composition & Product Characteristics
Each tablet contains 500 mg of paracetamol together with formulation-specific excipients required for manufacturing, stability and tablet performance. Technical evaluation should cover identification, assay, related substances, dissolution, disintegration, uniformity of dosage units, microbial quality and packaging integrity against the approved finished-product specification. Tablet appearance, excipient composition, pack configuration and storage requirements must be confirmed from the manufacturer’s product dossier and batch documentation.
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Additional Information
Formulation Application & Compatibility
Paracetamol Tablets 500mg is part of our Pharmaceutical Products range for pharmaceutical distributors, wholesalers, healthcare procurement teams and regulated-market buyers. Each oral tablet contains 500 mg of paracetamol, an analgesic and antipyretic ingredient used in products intended for the symptomatic relief of pain and fever. Buyers should match the offered dosage form, pharmacopoeial specification, excipient profile, packaging and labelling with their market-registration, distribution and tender requirements. The product must be supplied and used according to its approved labelling and applicable healthcare guidance.
- Country of Origin: Confirm from the manufacturer or supplier
- Regulatory/Pharmacopoeial Compliance: Confirm the applicable BP, Ph. Eur., USP or destination-market standard from the finished-product specification
- 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 a Paracetamol Tablets 500 mg Procurement Quote
Frequently Asked Questions
- What are the minimum order quantities and bulk order options for Paracetamol Tablets 500 mg? Minimum order quantities depend on the manufacturer, pack size, packaging configuration and destination-market requirements. Buyers should provide their required volume and delivery schedule to confirm available bulk-order options.
- How is pricing structured for large-volume Paracetamol Tablets 500 mg purchases? Pricing may vary according to order quantity, packaging format, documentation requirements, destination and shipment terms. Share the required quantity, pack configuration and Incoterm to obtain an appropriate commercial quotation.
- Are COA and pharmacopoeial documents available for this product? Documentation availability should be verified before ordering. Buyers may request the batch COA, finished-product specification, manufacturing authorization, stability information and other documents needed for registration, tendering or import clearance.
- What logistics and lead-time considerations apply to shipments? Lead time depends on production availability, batch-release testing, selected packaging, documentation and destination-country import procedures. Transportation and storage should follow the conditions stated on the approved product label.
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