About ESCITALOPRAM OXALATE IP
Escitalopram is used to treat depression and generalized anxiety disorder (GAD). It is an antidepressant that belongs to a group of medicines known as selective serotonin reuptake inhibitors (SSRIs). These medicines work by increasing the activity of the chemical serotonin in the brain.Exceptional Purity and ComplianceEscitalopram Oxalate IP meets rigorous pharmaceutical standards, with purity levels of 99% and all impurities within pharmacopeial limits. Each batch undergoes detailed identification procedures, including IR and HPLC tests, to ensure consistent quality and compliance with the Indian Pharmacopoeia regulations.
Optimized Storage and PackagingThe product is packed securely in double polyethylene bags within aluminum drums, offering robust protection against moisture and light. For optimal stability and shelf life, it should be stored between 2C to 8C. This advanced packing ensures product integrity from manufacturer to end-user.
Pharmaceutical Application BenefitsAs a key active ingredient, Escitalopram Oxalate IP is extensively utilized in formulations for depression and anxiety treatment. Its micronized and high-assay form benefits pharmaceutical manufacturers by ensuring reliable efficacy, ease of formulation, and compliance with strict quality parameters.
FAQ's of ESCITALOPRAM OXALATE IP:
Q: How should Escitalopram Oxalate IP be stored to maintain its efficacy?
A: Escitalopram Oxalate IP should be stored at temperatures between 2C and 8C, protected from moisture and light, to preserve its stability and potency throughout its 36-month shelf life.
Q: What are the primary uses of Escitalopram Oxalate IP in the pharmaceutical industry?
A: This API is predominantly used in the formulation of medications for Major Depressive Disorder and Generalized Anxiety Disorder, providing proven treatment benefits as an antidepressant.
Q: How is Escitalopram Oxalate IP identified and tested for quality?
A: Quality checks include standard identification methods such as Infrared Spectroscopy (IR) and High Performance Liquid Chromatography (HPLC), ensuring compliance with India's pharmacopoeial standards.
Q: When can manufacturers expect the product to remain within specification?
A: With correct storage conditions, Escitalopram Oxalate IP remains within pharmacopeial specifications for up to 36 months from the date of manufacture.
Q: Where is Escitalopram Oxalate IP manufactured and how is it packaged for delivery?
A: It is produced in India and packaged in double polyethylene bags placed in aluminum drums, safeguarding the compound during handling and transportation.
Q: What benefits does the pharmaceutical grade of Escitalopram Oxalate IP offer for drug formulation?
A: Its high purity, controlled particle size, and stringent quality parameters facilitate reliable formulation, resulting in consistent drug efficacy and compliance with regulatory standards.