Anadrolus 50 mg Driada Medical
$110.00
Driada Medical ANADROLUS provides pharmaceutical-grade Oxymetholone (Anadrol) standardized at 50 mg per oral tablet. Formulated for high oral bioavailability, this potent 17$\alpha$-alkylated DHT derivative is widely evaluated in laboratory research for its ability to drive rapid nitrogen retention, upregulate erythropoietin production, and stimulate significant muscle protein synthesis dynamics. Strictly for laboratory research use only.
Driada Medical ANADROLUS contains high-purity Oxymetholone standardized at 50 mg per tablet. Derived from dihydrotestosterone (DHT) with a modified 2-hydroxymethylene group, Oxymetholone is recognized as one of the most potent oral anabolic compounds in scientific research.
ANADROLUS is heavily studied in biochemical research models for its capacity to significantly increase red blood cell production via erythropoietin stimulation, enhance protein synthesis, and promote rapid nitrogen retention. Its 17-alpha-alkylated structure ensures high oral bioavailability, making it a foundational reference compound for studying severe tissue wasting recovery and acute anabolic response mechanisms.
Key Specifications
Ā Active Compound: Oxymetholone (Anadrol)
Ā Chemical Name: 17\beta\text{-hydroxy-2-hydroxymethylene-17}\alpha\text{-methyl-5}\alpha\text{-androstan-3-one}
Ā Molecular Formula: \text{C}_{21}\text{H}_{32}\text{O}_{3}
Ā Molecular Weight: 332.48\text{ g/mol}
Ā Concentration: 50 mg per tablet
Ā Formulation: Oral Tablets
Ā Manufacturer: Driada Medical
Ā Classification: 17$\alpha$-Alkylated Oral Anabolic Compound
Dosage & Research Protocol Guidelines
Ā Experimental Standard Dosage: In research and clinical evaluation models, standard reference protocols examine dosage ranges between 50 mg to 100 mg daily (1 to 2 tablets).
Ā Administration Frequency: Due to its active half-life of approximately 8 to 9 hours, daily administration is typically split into morning and evening doses to maintain steady plasma concentration.
Ā Research Duration: Protocol duration in animal and tissue models is typically restricted to 4 to 6 weeks due to 17$\alpha$-alkylated hepatic stress parameters.
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