Overview of Cospanon
| Property | Description |
|---|---|
| Active Ingredient | Flopropione |
| Form | Capsules |
| Pharmacological Class | Spasmolytic Agent (Antispasmodic) |
| General Purpose | Relief from visceral smooth muscle cramping |
| Origin | Synthetic (Propionic acid derivative) |
What Type of Medicine is Cospanon?
Cospanon is a pharmaceutical preparation classified as a spasmolytic agent, a type of medicine designed to relieve the involuntary contraction of smooth muscles within the body's internal systems. This drug is specifically designated as a selective visceral spasmolytic, meaning its action is concentrated on the viscera, or the internal organs, such as the ducts of the biliary and urinary systems. This selective approach is beneficial for mitigating the internal discomfort associated with cramping spasms. The drug is clinically recognized for its use in managing painful spasms, such as those that can accompany the passing of urinary calculus. This action reflects its role as a choleretic agent by promoting the flow of bile and pancreatic juice; this medicine helps ease discomfort by targeting the muscular source of the cramping pain.
Active Ingredient and Compositional Identity
The identity of the Cospanon brand is defined by its sole active component, Flopropione (2',4',6'-trihydroxypropiophenone), which is contained within the standard capsule form intended for oral administration. Flopropione is a synthetic compound, classified as a propionic acid derivative. While Flopropione is available under several trade names globally, the specific brand Cospanon is most widely established in the Japanese pharmaceutical market. Being a single-component product, Cospanon provides a clear mechanism of effect attributed entirely to Flopropione. Physiological actions include stimulating the flow and excretion of both bile and pancreatic juice, further contributing to the relief of pressure and promoting functional movement within the biliary and pancreatic tracts.
Regulatory References





