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Summary Of Ocriplasmin-API-Small Molecules

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Chemical Name

Ocriplasmin

CAS No.

1048016-09-6

Molecular Formula

C1214H1890N338O348S14

Innovator

Developer

Indication

Retinal Vein Occlusion; Vitrectomy

Therapeutic Area

Ophthalmology; Diagnostic, Therapeutic Techniques & Equipment

Market Status

Investigational

Approval Year

Patent Expiry

Looking for Detailed Summary of Ocriplasmin?

Chemxpert provides a consolidated intelligence snapshot for Ocriplasmin, covering its technical profile, commercial footprint, global Ocriplasmin supplier, Ocriplasmin buyer and Ocriplasmin 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 Ocriplasmin

Ocriplasmin 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 Ocriplasmin.

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

Commercial & Market Indicators for Ocriplasmin

Commercial & Market Indicators reflects the sales performance of Ocriplasmin–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 Ocriplasmin in major drug markets.

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

Global Supplier Landscape for Ocriplasmin

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

  • Ocriplasmin API Suppliers – Companies involved in the manufacturing or commercial supply of Ocriplasmin
  • 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
  • Ocriplasmin 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 Ocriplasmin

On the demand side, Ocriplasmin 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 Ocriplasmin API buyer contact records

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

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

Regulatory Filings & Market Authorization for Ocriplasmin

Ocriplasmin 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 Ocriplasmin 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 Ocriplasmin Regulatory, Commercial and Geographic Distribution – Click here

Clinical, Patent & Compliance Intelligence for Ocriplasmin

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 Ocriplasmin Clinical, Patent & Compliance – Click here

Biosimilar & Agrochemical Regulatory Status for Ocriplasmin

Chemxpert tracks biosimilar and agrochemical regulatory activity related to Ocriplasmin 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 Ocriplasmin 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.