Composition & Specifications
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What is Satdox-500 – Vancomycin Hydrochloride for Injection IP
\nSatdox-500 is Vancomycin Hydrochloride for Injection IP, a glycopeptide antibiotic used to treat serious and life-threatening gram-positive bacterial infections. It is especially effective against resistant organisms such as MRSA (Methicillin-Resistant Staphylococcus aureus). Due to its strong antibacterial profile, it is widely used in hospitals and intensive care settings. \n
How Vancomycin Injection Works
\nVancomycin works by inhibiting bacterial cell wall synthesis in gram-positive bacteria. It prevents the formation of the protective cell wall, leading to bacterial destruction. Unlike many other antibiotics, Vancomycin is particularly useful when infections do not respond to beta-lactam antibiotics. \n \nIts targeted action makes it a critical option in the management of resistant infections. \n
\nSatdox-500 is commonly prescribed for: \n
- Septicemia (bloodstream infections)
- Endocarditis
- Severe skin and soft tissue infections
- Bone and joint infections
- Hospital-acquired pneumonia
- MRSA infections
\nIt is administered intravenously under strict medical supervision for optimal results. \n
Vancomycin Hydrochloride Injection Key Benefits
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- Highly effective against resistant gram-positive bacteria
- Trusted therapy for MRSA infections
- Suitable for severe and hospital-acquired infections
- Reliable ICU-grade antibiotic
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Dosage Information
\nSatdox-500 should be administered slowly via intravenous infusion as directed by a healthcare professional. Kidney function monitoring is important during therapy, as dosage adjustments may be required in renal impairment. \n \nPatients should complete the prescribed treatment course to prevent antibiotic resistance and ensure effective recovery. Satdox-500 provides dependable and potent antibacterial coverage for serious infections requiring advanced care.
📋 Certificate of AnalysisBatch-specific CoA from NABL-accredited lab available for every product.
🏅 GMP Schedule MManufactured under Drugs & Cosmetics Act GMP Schedule M standards.
🔬 Third-Party TestedEvery batch independently tested by NABL-accredited laboratory before dispatch.
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Prescribing & Administration Information
⚠️ For Healthcare Professionals & Franchise Partners Only: This product is sold through licensed PCD franchise partners and authorised stockists. Prescribing, dosage, and administration information is available in the product literature and Patient Information Leaflet (PIL) supplied with each batch.
Dosage & Administration
As directed by the prescribing physician. Dosage varies by indication, patient age, and clinical condition. Full prescribing information included with product.
Storage Conditions
Store in a cool, dry place below 25°C, away from direct sunlight and moisture. Keep out of reach of children. Do not use after expiry date printed on the pack.
Available Documentation
📄Product Information Leaflet (PIL) — included with every batch
🔬NABL-accredited Certificate of Analysis (CoA) — available on request per batch
📋Drug License compliance documents — provided with franchise agreement
🏅WHO-GMP manufacturing certificate — available for regulatory submission
