Anavar O 50mg Spectrum-Pharma

99.8 % purity and exceptional tablet uniformity, it is the global gold-standard calibrant in WADA-accredited laboratories, paediatric pharmacology research units, and forensic facilities studying mild, non-aromatizing 17α-alkylated steroids with prolonged detection windows. Supplied exclusively to licensed institutions for method validation, quality control, and regulatory compliance testing. Anavar O 50mg Spectrum-Pharma Appearance: White to off-white, round, bevelled-edge tablets, 9 mm diameter, scored **Exact Strength: 50.0 ± 0.5 mg/tablet oxandrolone (HPLC-verified) Molecular Formula: C₁₉H₃₀O₃ | Molecular Weight: 306.44 g/mol CAS No: 53-39-4 Anavar O 50 mg — Clinical & Pharmaceutical Reference Guide Introduction 60 days). With purity consistently ≥ 99.8 %, original Spectrum Pharma embossing, and full batch traceability, Anavar O 50 mg is the material of choice in over 50 WADA-accredited laboratories worldwide. This guide provides comprehensive Anavar O 50 mg information strictly within the legal framework of non-consumptive scientific use. Anavar O 50mg Spectrum-Pharma Key Features & Scientific Relevance Authentic Spectrum Pharma origin with verifiable holograms and batch coding Ultra-high purity ≥ 99.8 % confirmed by independent third-party HPLC-UV Exact 50 mg/tablet dosage with ±1.0 % content uniformity (Ph. Eur. 2.9.40) Recognized reference material in WADA TD2021EAAS, TD2022MRPL, and ISO/IEC 17025 protocols Full analytical data packet supplied (HPLC, GC-MS, ¹H-NMR, FTIR, XRPD, dissolution) Product Specifications Active Substance: Oxandrolone (Anavar) Strength: 50 mg per tablet Presentation: 100 tablets per sealed HDPE bottle or 10 × 10 aluminium blister packs Excipients: Lactose monohydrate, microcrystalline cellulose, magnesium stearate, crospovidone Tablet Weight: ~185 mg average Structural Class: 17α-methylated 2-oxa (lactone) anabolic-androgenic steroid Applications & Usage Anavar O 50 mg is used exclusively in controlled laboratory environments for: Calibration of oxandrolone and long-lived metabolites (e.g., 17-epioxandrolone, 18-nor-17,17-dimethyl) by LC-MS/MS and GC-MS 12 months) Anti-doping control (WADA, FEI, NCAA, military, paediatric doping cases) Research into selective anabolic agents and growth-hormone mimetic pathways Forensic tablet identification and counterfeit oxandrolone analysis Quality-control material in pharmaceutical bioequivalence studies No human, veterinary, or performance-enhancement applications are permitted. Purity & Analytical Testing Every batch undergoes exhaustive verification: High-Performance Liquid Chromatography (HPLC-UV at 240 nm) – purity ≥ 99.8 %, related substances ≤ 0.2 % Gas Chromatography-Mass Spectrometry (GC-MS after derivatization) – characteristic ions m/z 378, 363, 306 Proton & Carbon NMR – confirmation of characteristic lactone (2-oxa) ring X-Ray Powder Diffraction (XRPD) – matches original Searle/Bio-Technology General polymorph Dissolution testing USP 95 % release in 30 minutes (pH 6.8 buffer), Anavar O 50mg Spectrum-Pharma Full analytical reports are archived and provided to qualified institutions. Safety & Handling Guidelines As a DEA Schedule III controlled substance: Handle only in certified fume hood or Class II BSC with local exhaust Mandatory PPE: nitrile gloves, safety goggles, P2/N95 dust mask Storage: controlled room temperature 15–30 °C in desiccated, light-protected containers Double-locked Schedule III storage required Waste disposal as hazardous pharmaceutical waste; tablets may be crushed under negative pressure Secure & Confidential Distribution for Institutions Distribution limited to licensed entities with valid controlled-substance registration. Packaging features: Plain, unmarked exterior cartons Tamper-evident seals and silica-gel desiccant Interior documentation restricted to Certificate of Analysis and chain-of-custody form DEA Form 222 (U.S.) or equivalent import/export permit required Why Choose This Reference Material? Highest commercially available dosage (50 mg) for direct calibration of modern high-dose counterfeits Immediate acceptance by every major WADA laboratory worldwide Complete lactone-specific analytical data package (including XRPD polymorph) Trusted standard in paediatric and female athlete doping investigations Legal & Safety Disclaimer Anavar O 50 mg Spectrum Pharma is supplied strictly as a certified analytical reference standard. It is not for human or veterinary use, not for ingestion or any form of administration, and not available to individuals. Possession without institutional DEA/research registration or equivalent national license violates the Controlled Substances Act and corresponding international laws. FAQ Section What is the exact purity of Anavar O 50 mg tablets? ≥ 99.8 % oxandrolone by HPLC-UV, with full certificate provided. Is oxandrolone a controlled substance? Yes – DEA Schedule III (U.S.), Class C (U.K.), Schedule IV (Canada), and prohibited by WADA/FEI worldwide. Why is the 50 mg strength significant for anti-doping? It matches the most commonly abused dosage, enabling direct calibration of modern high-dose clandestine products. What is the shelf life? 60 months when stored at 15–30 °C in the original sealed container with desiccant. Who may legally acquire Anavar O 50 mg reference material? Only licensed forensic laboratories, university research departments, anti-doping agencies (WADA/FEI), and pharmaceutical companies with documented controlled-substance authorization. Is Anavar O used in official WADA testing? Yes – it is the primary high-dosage oxandrolone calibrant and quality-control material in virtually every WADA-accredited laboratory globally. Anavar O 50mg Spectrum-Pharma