TAMOXIFEN 30ML X 20MG

Description

Tamoxifen is a selective estrogen receptor modulator (SERM) that has been widely used in clinical medicine and research settings. It is primarily known for its role in regulating estrogen receptor activity in various tissues, and it has been extensively studied in both medical and scientific contexts.

In clinical practice, tamoxifen is most commonly used under medical supervision as part of treatment protocols for hormone receptor-positive breast cancer. It works by binding to estrogen receptors and modulating their activity, which can influence estrogen-dependent cellular growth pathways. Its effects vary depending on the tissue type, acting as an antagonist in some tissues and a partial agonist in others.

The 30ml x 20mg formulation typically refers to a liquid concentration format used in controlled dispensing environments. Standardized concentrations are important in clinical and research contexts to ensure accurate dosing, measurement consistency, and reproducibility in studies or treatment protocols.

Research involving tamoxifen has also contributed significantly to the understanding of estrogen receptor signaling, endocrine regulation, and gene expression modulation. Because of its well-characterized mechanism of action, it is frequently used as a reference compound in molecular biology and pharmacology research.

Manufactured pharmaceutical-grade tamoxifen is produced under strict quality control standards, including identity verification, purity testing, and batch consistency checks. These measures ensure safety, reliability, and compliance with regulatory requirements in clinical and research environments.

Proper storage and handling are essential to maintain stability and effectiveness. Tamoxifen should be stored according to manufacturer guidelines and handled in accordance with applicable pharmaceutical and laboratory standards.

Tamoxifen is intended strictly for prescription use under medical supervision or controlled research settings. It is not intended for unsupervised use, and all applications should comply with applicable laws, regulations, and institutional protocols.