Human Formulations

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AU Film-Coated Tablet

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AU Film-Coated Tablet is a film-coated tablet formulated with Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AU. The active ingredient profile is Aceclofenac; Par

TabletsNon-Beta-Lactam Tablets Single Ingredient Film-Coated Tablet
Sterile injectable formulation

Product information

Product Line
Human Formulations
Category
Tablets, Non-Beta-Lactam Tablets
Dosage Form
Film-Coated Tablet
Product Type
Single Ingredient

Available strengths

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AUAceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 1 Lac AU

Description

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AU Film-Coated Tablet is a film-coated tablet formulated with Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 AU. The active ingredient profile is Aceclofenac; Paracetamol; Trypsin-Chymotrypsin, placing the product in the nsaid + analgesic + proteolytic enzyme combination category. The formulation combines analgesic/anti-inflammatory ingredients with proteolytic enzyme components commonly used as adjuncts in clinician-managed inflammatory or soft-tissue conditions. The film coating provides a finished oral solid-dosage presentation and may support handling, stability and product acceptability. For website cataloguing, composition, strength, dosage form and release/coating characteristics should be displayed prominently and consistently. The description should remain factual and should not include unapproved cure, superiority, guaranteed-result or broad therapeutic claims. Clinical selection should depend on diagnosis, patient-specific factors, contraindications, concomitant medicines and the prescriber’s judgement. Prescription status, precautions, interactions, adverse effects and dosing must be checked against the current approved product label before publication. Manufacturer, licence, storage, shelf-life, pack configuration and market-specific regulatory details should be added only from verified product documentation.
WHO-GMP Sourced
Sterile Supply
Regulatory Documentation
Quality Assured