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Summary Of Emedastine-API-Small Molecules

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Chemical Name

Emedastine

CAS No.

87233-61-2

Molecular Formula

C17H26N4O

Innovator

Developer

Indication

Allergic Conjunctivitis; Allergic Rhinitis

Therapeutic Area

Ophthalmology; Immunology

Market Status

Launched

Approval Year

Patent Expiry

Detailed Summary of Emedastine API-Small Molecules

Chemxpert provides a consolidated intelligence snapshot for Emedastine API-Small Molecules, covering its technical profile, commercial footprint, global Emedastine supplier, Emedastine buyer and Emedastine manufacturer dynamics, and regulatory presence across key pharmaceutical markets.

Innovator and developer details, where available, are reflected based on verified disclosures within Chemxpert database.

Technical & Application Intelligence for Emedastine

Emedastine technical & application intelligence includes information on the industry and end-use applications, helping users understand its role across different formulation and therapeutic contexts. The data also covers routes of synthesis and manufacturing technologies, offering visibility into production methods, process variability, and technical complexity.

In addition, the mechanism of action describes how an API ingredient produces its therapeutic effect at the molecular or biological level in the body. This data supports scientific understanding, formulation development, and regulatory evaluation of Emedastine.

Chemxpert tracks the technical landscape of Emedastine across its manufacturing and application ecosystem.

Commercial & Market Indicators for Emedastine

Commercial & Market Indicators reflects the sales performance of Emedastine–based products across key pharmaceutical markets, including regulated regions such as the United States and the United Kingdom where available. It helps users understand regional demand trends, market maturity, and commercial presence of Emedastine in major drug markets.

  • Emedastine global market size is tracked in both volume (metric tonne) and value (USD)
  • Pricing intelligence includes average Emedastine API price benchmarks (USD/kg) derived from multiple verified sources
  • Regional Emedastine API sales performance including markets such as the US and UK is monitored where data is available

Global Supplier Landscape for Emedastine

Emedastine global supplier landscape provides intelligence on the API global supply ecosystem, helping users identify manufacturers, assess supply scale, and evaluate regulatory readiness.

  • Emedastine API Suppliers – Companies involved in the manufacturing or commercial supply of Emedastine
  • Supplying Volume – Indicator of quantity supplied used to assess production scale and capacity
  • Supplier Country Presence – Geographic distribution across countries
  • Supplier Regulatory Certifications – GMP, FDA and other approvals held by facilities
  • Emedastine API Verified Supplier Contact Information – Validated business contact details

Together, this supplier intelligence supports supplier discovery, qualification, diversification planning, and supply risk assessment. This dataset supports supplier qualification, diversification planning, and sourcing risk mitigation.

Buyer & Demand Intelligence for Emedastine

On the demand side, Emedastine API buyer supplier data intelligence tracks global procurement activities.

  • Total identified buyers across the globe
  • Total buying volume in metric tonne
  • Buyer presence across countries
  • Total number of certified buyers
  • Verified Emedastine API buyer contact records

This intelligence enables demand mapping, partner discovery, and market entry evaluation.

Get the detailed insight about Emedastine technical, commercial, supplier and buyer –Click here

Regulatory Filings & Market Authorization for Emedastine

Emedastine regulatory filings & market authorization provide a comprehensive view of approval status across global pharmaceutical markets.

  • US Drug Master File (US-DMF)
  • FDA National Drug Code (NDC)
  • Certificate of Suitability (CEP / COS)
  • EU API Registration
  • UK-MHRA Registration
  • REACH Registration
  • Written Confirmation

Asia-Pacific & Other Regional Filings

  • Japan Drug Master File (J-DMF)
  • Korea Drug Master File (K-DMF)
  • India Import Licence
  • China API Registration
  • Other regional registrations (Middle East, Africa, Latin America)

Finished Dosage Form (FDF) Market Authorization

  • North America
  • Europe
  • Oceania
  • Africa
  • Asia
  • South America

Geographic Distribution of Emedastine Counterparties

  • North America
  • Europe (Northern, Western, Southern, Eastern)
  • Asia
  • Africa
  • Middle East
  • South America
  • Oceania

Country-level counts are dynamically populated to reflect real-time database coverage.

Get the detailed insight about Emedastine Regulatory, Commercial and Geographic Distribution –Click here

Clinical, Patent & Compliance Intelligence for Emedastine

Clinical Trial Activity

Tracks ongoing and completed trials across the US, Europe, Asia-Pacific and India.

Patent & Exclusivity Landscape

  • Patent expiry
  • Market exclusivity
  • SPC extensions
  • Paragraph IV filings
  • Patent disputes & data protection

Certifications & Accreditations

  • US FDA
  • EU GMP
  • PMDA (Japan)
  • ANVISA (Brazil)
  • CDSCO, WHO-GMP, PIC/S

Regulatory Warnings & Compliance Signals

  • FDA warnings and recalls
  • Form 483 observations
  • Site inspection records
  • Country bans, price controls and essential medicine listings

Get detailed insight on Emedastine Clinical, Patent & Compliance –Click here

Biosimilar & Agrochemical Regulatory Status for Emedastine

Chemxpert tracks biosimilar and agrochemical regulatory activity related to Emedastine across global markets. A regulatory dashboard reflects filing and approval status in the US, Europe, Japan, India, China and other countries.

Get detailed Biosimilar & Agrochemical Regulatory Insight – Click here

Why Use Chemxpert for Emedastine API Intelligence?

Chemxpert combines supplier data, regulatory depth, commercial indicators, US DMF and compliance intelligence into a single continuously updated platform — helping pharmaceutical companies, buyers and regulators make faster and better-informed decisions.