Description

Eskornade Spansules is a specialized pharmaceutical formulation designed for controlled-release delivery. This product is critical for ensuring consistent therapeutic levels and improving patient compliance in treatment regimens. It is primarily utilized by the pharmaceutical industry for the development and production of extended-release oral dosage forms. The compound is identified by the CAS registry number 77306-14-0.

Application

• Core component in the manufacture of controlled-release (Spansule®) capsule formulations.
• Used in pharmaceutical R&D for developing sustained-release oral solid dosage forms.
• Application in combination drug therapies requiring timed release of active ingredients.
• Potential excipient or intermediate in specialty generic and novel drug delivery systems.
• Used for clinical trial material production for extended-release studies.
• Serves as a reference standard for quality control and analytical method development in pharmaceutical labs.

Basic Information

Product Name	Eskornade Spansules
CAS No.	77306-14-0
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Eskornade; Eskornade Spansule; Controlled-Release Eskornade; Timed-Release Eskornade Formulation; 77306-14-0; Eskornade SR; Eskornade Extended-Release Capsules
EINECS	Contact for details

Quality Control

Our Eskornade Spansules are manufactured under strict quality systems suitable for pharmaceutical use. The product undergoes rigorous analytical testing to ensure identity, purity, potency, and consistent release profile. A comprehensive Certificate of Analysis (COA) is provided with each batch, detailing results against predefined specifications for critical quality attributes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Maintain in original packaging until use to protect integrity.

Specification

Item	Specification
Appearance	White to off-white pellets/spheres
Identification (IR)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0%
Dissolution Profile	Meets controlled-release criteria
Uniformity of Dosage Units	Conforms to Ph. Eur./USP
Related Substances (HPLC)	NMT 1.0% total impurities
Residual Solvents (GC)	Conforms to ICH Q3C
Water Content (KF)	NMT 3.0%
Microbial Limits	Conforms to Ph. Eur./USP <61>, <62>

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.