Stability of hydroxyprogesterone caproate alone and in a compounded pharmaceutical product.
Purpose. The chemical stability of hydroxyprogesterone caproate in powder form and in a pharmaceutical formulation under different experimental conditions was evaluated. Methods. Pure hydroxyprogesterone caproate was subjected to hydrolysis, photolysis, and thermal degradation. The content of hydrox...
| Published in: | American Journal of Health-System Pharmacy Vol. 71; no. 13; pp. 1120 - 1128 |
|---|---|
| Main Authors: | , , , |
| Format: | research tables/charts Journal Article |
| Published: |
Oxford University Press / USA
7/1/2014
|
| Online Access: | View this record in EBSCOhost |