Paracetamol Effervescent 500mg Tablets

Paracetamol Effervescent Tablets 500 MG
  • Dosage: Paracetamol 500mg
  • Packaging: 5 tablets/blister*5/box
  • Shelf Life: 36months 

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Product Description

Product NameParacetamol Effervescent Tablets (Paracetamol 500mg Effervescent Oral Tablets)
SpecificationEach effervescent tablet contains: Paracetamol 500mg
Dosage FormEffervescent Tablet (for oral administration after dissolution in water)
Active IngredientParacetamol (Acetaminophen)
Pharmacological ClassAnalgesic / Antipyretic (Non-Opioid)
Route of AdministrationOral administration after dissolution. Dissolve one effervescent tablet in a glass of water (approximately 200mL), wait until completely dissolved, then drink the solution. Do NOT swallow the tablet whole.
PackagingTube pack (plastic tube with desiccant cap) or blister pack, typically 20 or 10 tablets per tube/box
StorageStore below 25°C, in a dry place, protected from light and moisture. Keep tube tightly closed with desiccant cap in place. Do not remove desiccant from the tube. Do not freeze.
Shelf Life36 months (unopened); use within 3 months of first opening the tube

Product Overview

Paracetamol Effervescent Tablets is an oral analgesic and antipyretic preparation containing Paracetamol 500mg per effervescent tablet. Paracetamol is a widely used non-opioid analgesic and antipyretic agent. The effervescent formulation is designed to dissolve completely in water before ingestion, producing a palatable solution that is easier to swallow than conventional tablets. This formulation is particularly suitable for patients who have difficulty swallowing tablets or capsules, such as the elderly, children (when age-appropriate), and patients with dysphagia. The effervescent formulation also provides faster absorption compared to conventional solid oral dosage forms.

Paracetamol Effervescent 500mg Tablets: What the Published Guidance Says

The three non-opioid analgesics named on the WHO Model List — paracetamol, ibuprofen and acetylsalicylic acid — in the full range of oral, rectal and injectable presentations, plus the wider NSAID family.

Buyers usually settle three things before ordering Paracetamol Effervescent 500mg Tablets: the pharmacopoeial monograph, the pack configuration, and the documents the destination authority will ask for.

We quote these sources rather than paraphrase them loosely, because the detail matters commercially for Paracetamol Effervescent 500mg Tablets. Where your national list differs from the WHO listing, the national list governs what may be supplied and promoted locally.

Ordering Parameters for Paracetamol Effervescent 500mg Tablets

Product NameParacetamol Effervescent Tablets (Paracetamol 500mg Effervescent Oral Tablets)
SpecificationEach effervescent tablet contains: Paracetamol 500mg
Dosage FormEffervescent Tablet (for oral administration after dissolution in water)
Active IngredientParacetamol (Acetaminophen)
Pharmacological ClassAnalgesic / Antipyretic (Non-Opioid)
Route of AdministrationOral administration after dissolution. Dissolve one effervescent tablet in a glass of water (approximately 200mL), wait until completely dissolved, then drink the solution. Do NOT swallow the tablet whole.
StorageStore below 25°C, in a dry place, protected from light and moisture. Keep tube tightly closed with desiccant cap in place. Do not remove desiccant from the tube. Do not freeze.
Therapeutic groupAnalgesics & NSAIDs — Analgesics & NSAIDs
ManufacturerSinophare Bio-technology Co., Ltd. (GMP, China)
Documentation suppliedCOA, HPLC/GC data, stability data, dossier package

The same therapeutic range is supplied in several presentations, so one purchase order can cover a mixed requirement: Aspirin 300mg Tablets, Paracetamol Diphenhydramine Chlorphenamine Tablets, Ibuprofen 100mg Tablets, Methamizole 500mg Tablets, Paracetamol 500mg Tablets, Ibuprofen Suppository 50mg, Indomethacin Suppository 100mg, Naproxen Suppositories 250mg.

Pharmacopoeial Standard, Release Testing & COA

Products are manufactured and tested against USP, EP, BP and CP monographs, with incoming raw-material inspection, in-process monitoring and full finished-product testing.

Every batch of Paracetamol Effervescent 500mg Tablets is tested to the monograph stated on the purchase order. Where a monograph is silent on the presentation, we agree a written specification with you in advance and reference it on the certificate of analysis.

Standardised GMP production workshops with an independent R&D laboratory and a complete quality-inspection centre.

The quality control package for the marketed pack covers:

  • Testing for assay of the active substance
  • Testing for related substances and impurities
  • Testing for dissolution or release profile (solid oral forms)
  • Testing for uniformity of dosage units
  • Testing for water content and pH where applicable
  • Testing for sterility and bacterial endotoxins (parenterals and ophthalmics)

COA, HPLC and GC data, DMF and dossier packages, plus registration support documents for national marketing-authorisation filings.

Packing, Labelling Languages & Export Paperwork

  • Pack size: Tube pack (plastic tube with desiccant cap) or blister pack, typically 20 or 10 tablets per tube/box. Non-standard pack sizes can be quoted against your artwork.
  • Storage: Store below 25°C, in a dry place, protected from light and moisture. Keep tube tightly closed with desiccant cap in place. Do not remove desiccant from the tube. Do not freeze..
  • Shelf life: 36 months (unopened); use within 3 months of first opening the tube. Stability data for the marketed pack is included in the dossier.
  • Labelling: we typeset the carton and leaflet in English, Arabic, French, Russian and Spanish and in any further language your market requires, carrying your own brand where the local rules allow.
  • Export: commercial invoice, packing list, certificate of origin, GMP certificate, COA and the free-sale certificate issued by the country of manufacture whenever your customs or regulator asks for it.

Marketing Authorisation & Tender Support

Documents for Paracetamol Effervescent 500mg Tablets are issued by Sinophare Bio-technology Co., Ltd. — DML Number Jin20160068 (medicines) and Jin20160069 (paracetamol API).. Keeping one legal manufacturer across the COA, the GMP certificate and the registration file avoids assessment queries later.

  • Answers to authority questions during assessment, handled by the regulatory contact who prepared the file.
  • Tender and framework documentation, including pre-qualification questionnaires and sample logistics.
  • Artwork and mock-up approval pack, showing the carton, label and leaflet exactly as they will be printed for your market.
  • Batch manufacturing and packaging records released for inspection on request during supplier audits.
  • Re-test or renewal support when the marketing authorisation comes up for variation or renewal.

The context for Paracetamol Effervescent 500mg Tablets is its place among non-opioid analgesics and NSAIDs named in the WHO Model List. Listing status informs how programmes specify a product; it is not a substitute for the import licence or marketing authorisation of the destination country.

Paracetamol Effervescent 500mg Tablets: Common Procurement Questions

What pack size is available for Paracetamol Effervescent 500mg Tablets?

This presentation is normally supplied as Tube pack (plastic tube with desiccant cap) or blister pack, typically 20 or 10 tablets per tube/box. Where your market requires a different count, bottle or carton, we quote to your artwork and extend the stability file to the new pack.

What documentation comes with a shipment of Paracetamol Effervescent 500mg Tablets?

Shipments are accompanied by a certificate of analysis covering identification, assay and related substances, together with the marketed-pack stability data and the manufacturing site GMP certificate. Shelf life: 36 months.

Does the batch documentation for Paracetamol Effervescent 500mg Tablets support a registration filing?

Shipments are accompanied by a certificate of analysis covering identification, assay and related substances, together with the marketed-pack stability data and the manufacturing site GMP certificate. Shelf life: 36 months. The full CTD dossier and the authority assessment file are supplied as part of a registration order; routine shipments carry the COA and stability data only.

Can you supply sustained-release or combination analgesics?

Yes — including compound presentations and sustained-release forms. Confirm the specific combination against your national registration before ordering.

Which strengths of paracetamol oral liquid should we order?

The WHO Model List notes that offering both 120 mg/5 mL and 125 mg/5 mL on one market causes prescribing and dispensing confusion. We recommend selecting one strength per market and will supply accordingly.

Products Commonly Ordered with Paracetamol Effervescent 500mg Tablets

Browse the full Analgesics & NSAIDs range; all Tablets; the complete product catalogue.

Request a Quotation for Paracetamol Effervescent 500mg Tablets

For tenders and programme supply, send the line item, pack size, quantity and destination for Paracetamol Effervescent 500mg Tablets 500mg. We return a quotation with lead time, documentation list and sample availability in one response.

Request a quotation

Sources & Regulatory Notes

Reference information only. The published guidance summarised on this page is quoted for professional and regulatory-context purposes and does not constitute medical advice, a prescribing recommendation or a promotion of any product for a particular indication. Prescribing decisions must follow the approved product information and national treatment guidelines in the market of use.

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