Comprehensive
Dosage Form Capabilities
Austex Pharma delivers high-quality pharmaceutical formulations across a diverse range of dosage forms, designed for global markets and patient needs.
Our manufacturing capabilities are designed to support a wide spectrum of dosage forms, ensuring flexibility, precision, and compliance across therapeutic categories and markets.
Formulation Portfolio
Precision-focused delivery systems tailored for maximum therapeutic efficacy.
Tablets
Precision-engineered solid dosage forms designed for stability and effectiveness.
Capsules
Encapsulated formulations ensuring accurate dosing and patient compliance.
Syrups / Liquid Orals
Palatable and effective liquid formulations for diverse patient groups.
Suspensions
Uniform and stable suspensions for controlled delivery.
Injectables
Sterile, high-quality formulations for critical therapeutic applications.
Powders / Sachets
Flexible and convenient formats for varied dosing needs.
Ointments / Topicals
Targeted formulations for localized treatment and skin absorption.
Integrated Manufacturing Excellence
Our facilities leverage high-speed automated lines and closed-system processing to ensure absolute sterility and batch-to-batch consistency. We integrate real-time monitoring and advanced filtration systems to meet the most stringent pharmaceutical standards.
Lifecycle of Precision
From concept to global distribution, every phase is governed by scientific rigour.
Formulation
Initial blending and active ingredient optimization.
Testing
In-process checks for density, viscosity, and potency.
Validation
Compliance verification against Pharmacopoeia standards.
Manufacturing
Scalable production in GMP-controlled environments.
Packaging
Secure, tamper-evident and climate-stable finishing.
Advanced R&D Framework
Our scientists focus on the frontier of bioavailability and stability, ensuring every dosage form performs at its peak when it reaches the patient.
Bioavailability Optimization
Innovative carrier systems to enhance the solubility and absorption of challenging compounds.
Stability Testing
Accelerated and real-time ICH stability studies across all climatic zones.
Analytical Methods
Validated HPLC and GC methods for impurity profiling and assay testing.
Global Compatibility
Formulations designed for US-FDA, EU-GMP, and PICS regulatory readiness.