Human Formulations

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IU Tablet

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IU Tablet is a tablet formulated with Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IU. The active ingredient profile is Aceclofenac; Paracetamol; Trypsin-Chym

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

Product information

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

Available strengths

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IUAceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 50,000 IUAceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 75,000 IU

Description

Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IU Tablet is a tablet formulated with Aceclofenac 100 mg + Paracetamol 325 mg + Trypsin-Chymotrypsin 150,000 IU. 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 source identifies this item as a tablet product but does not specify a coating or release characteristic on that line. 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