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Indian Pharmaceutical Exporter Β· #7 for Teicoplanin Β· $101.2K export value Β· DGFT Verified
Sanofi India Limited is the #7 Indian exporter of Teicoplanin with $101.2K in export value and 6 verified shipments. Sanofi India Limited holds a 1.6% market share in Teicoplanin exports across 1 countries. The company exports 4 pharmaceutical products worth $9.0M across 4 therapeutic categories.

| Country | Value | Shipments | Share |
|---|---|---|---|
| SRI LANKA | $1.2M | 43 | 24.1% |
| HUNGARY | $1.1M | 23 | 24.0% |
| SOUTH AFRICA | $1.1M | 21 | 21.9% |
| GERMANY | $336.9K | 7 | 7.0% |
| RUSSIA | $250.0K | 5 | 5.2% |
| LEBANON | $215.0K | 34 | 4.5% |
| NEPAL | $152.3K | 16 | 3.2% |
| VENEZUELA | $121.7K | 9 | 2.5% |
| CUBA | $100.0K | 2 | 2.1% |
| SPAIN | $100.0K | 2 | 2.1% |
India exports Teicoplanin to 44 countries. The top destination is SRI LANKA (24.1%), followed by HUNGARY and SOUTH AFRICA.
| Buyer | Country | Value | Orders |
|---|---|---|---|
| SLIM PHARMACEUTICALS (PVT) LTD, | SRI LANKA | $245.7K | 14 |
| YADEN INTERNATIONAL (PVT) LTD | SRI LANKA | $215.1K | 5 |
| MEDPRO PHARMACEUTICA PTY LTD | SOUTH AFRICA | $209.1K | 6 |
| AUSTELL PHARMACEUTICALS (PTY) LTD, | SOUTH AFRICA | $195.1K | 4 |
| AUSTELL PHARMACEUTICALS ( PTY) LTD | SOUTH AFRICA | $150.0K | 3 |
| HANSE SERVICE INTERNATIONALE | GERMANY |
India exported $5.7M worth of Teicoplanin through 310 shipments from 60 suppliers to 44 countries, serving 108 buyers globally. Sanofi India Limited contributes $101.2K to this total, accounting for 1.6% of India's Teicoplanin exports.
Sanofi India Limited's average Teicoplanin shipment value is $16.9K per consignment, based on 6 shipments totaling $101.2K.
Sanofi India Limited ranks #7 among 60 Indian Teicoplanin exporters with a 1.6% market share. The top 3 exporters are GUFIC BIOSCIENCES LIMITED ($4.3M), FLAGSHIP BIOTECH INTERNATIONAL PRIVATE LIMITED ($250.0K), JODAS EXPOIM PRIVATE LIMITED ($250.0K). Sanofi India Limited processed 6 shipments to 1 destination countries.
What Sanofi India Limited must comply with to export Teicoplanin to its top destination countries
Approval Process
Registration under SAHPRA guidelines (CTD format). Bioequivalence required for generics.
Timeline: 24β48 months (significant backlog)
GMP & Export Requirements
WHO GMP or PIC/S GMP compliance
Certificate of Pharmaceutical Product from CDSCO; Import permit per Section 22A of Medicines Act
Note: Known registration backlog. WHO Prequalification significantly assists the process.
Approval Process
Marketing Authorisation via Decentralized or Mutual Recognition Procedure under EU Directive 2001/83/EC. CTD Module 1β5 dossier required.
Exporters ranked immediately above and below #7 by export value
| # | Supplier | Export Value | Shipments | Countries | Avg/Shipment |
|---|---|---|---|---|---|
| 5 | NEON LABORATORIES LIMITED | $215.1K | 6 | 2 | $35.8K |
| 6 | VENUS REMEDIES LIMITED | $134.1K | 18 | 9 | $7.4K |
| 7 | SANOFI INDIA LIMITED β | $101.2K | 6 | 1 | $16.9K |
| 8 | UNITED BIOTECH PRIVATE LIMITED | $91.2K | 19 | 8 | $4.8K |
| Port | Shipments | % Share |
|---|---|---|
| SAHAR AIR CARGO ACC (INBOM4) | 69 | 22.3% |
| SAHAR AIR | 67 | 21.6% |
| NHAVA SHEVA SEA (INNSA1) | 27 | 8.7% |
| DELHI AIR | 24 | 7.7% |
| Bombay Air | 22 | 7.1% |
| DELHI AIR CARGO ACC (INDEL4) | 16 | 5.2% |
| CHENNAI AIR CARGO ACC (INMAA4) | 8 | 2.6% |
| HYDERABAD AIR | 8 | 2.6% |
Recent geopolitical developments have introduced significant challenges for Indian pharmaceutical exporters like Sanofi India. The escalation of conflicts in the Middle East, particularly around the Red Sea and Suez Canal, has disrupted key shipping routes. Major carriers have suspended or restricted transits, leading to extended transit times by 10β20 days and increased freight rates by 40β50% on IndiaβEurope routes. (livemint.com) These disruptions pose risks to the timely delivery of temperature-sensitive pharmaceuticals, potentially affecting product efficacy and market competitiveness.
In the United States, the implementation of tariffs on pharmaceutical imports, including a 25% reciprocal tariff and an additional 25% penalty tied to India's energy policies, has created an uncertain trade environment. Although pharmaceuticals have been exempt from some of these tariffs, the potential for future escalations remains a concern. (en.wikipedia.org) Additionally, the European Union's stringent regulatory frameworks, such as the Falsified Medicines Directive, necessitate rigorous compliance measures, adding complexity to market entry and sustainability for exporters like Sanofi India.
Compliance with international regulatory standards is paramount for Indian pharmaceutical exporters. Sanofi India has consistently adhered to guidelines set by the U.S. Food and Drug Administration (FDA), the World Health Organization (WHO), and the European Union's Good Manufacturing Practices (EU GMP). This commitment ensures product quality and facilitates access to global markets. However, evolving regulatory requirements, such as the EU's Falsified Medicines Directive, demand continuous adaptation and investment in compliance infrastructure. For instance, the directive's serialization and traceability mandates require significant technological upgrades, impacting operational costs and necessitating strategic planning.
Sanofi India Limited exports 4 products worth $9.0M. Beyond Teicoplanin, top products include Ramipril, Codeine, Insulin. View the complete Sanofi India Limited profile for full portfolio analysis.
Latest developments and market context
Detailed market intelligence for Teicoplanin β including regulatory updates, trade policy changes, and competitive landscape analysis β will be available in an upcoming update. This section will feature AI-researched insights from verified industry sources, government notifications, and market reports.
Pharmaceutical Export-Import Analyst & Trade Intelligence Expert
Suresh Sormare is a pharmaceutical export-import analyst with deep expertise in Indian Customs (DGFT) data, HS code classification, and global pharmaceutical supply chains. His analysis covers 10M+ shipment records across 150+ countries and is used by manufacturers, procurement agencies, and trade consultants worldwide. Suresh specializes in identifying verified suppliers and buyers from customs records, mapping bilateral pharmaceutical trade corridors, analyzing tariff structures and regulatory frameworks across 170+ destination markets, and benchmarking competitive positioning for finished pharmaceutical formulations. His methodology combines granular customs transaction data with regulatory intelligence from FDA, EMA, WHO, CDSCO, and 40+ national drug authorities to deliver actionable trade insights for the pharmaceutical formulations sector.
linkedin.com/in/sureshsormareAll trade data is sourced from Indian Customs (DGFT) official shipping bill records β the authoritative government database for India's pharmaceutical trade. Each verified record contains exporter name, consignee (buyer) name, detailed product description, quantity, declared FOB value (USD), port of loading, destination country, and shipment date.
Access shipment-level details, pricing data, buyer connections, and competitive analysis for Sanofi India Limited's Teicoplanin exports. TransData Nexus provides verified Indian Customs (DGFT) data trusted by pharmaceutical trade professionals worldwide.
Sanofi India Limited
Full Company Profile β
4 products Β· $9.0M total trade Β· 4 categories
| $150.0K |
| 3 |
| MEDICUBA, S.A. | CUBA | $100.0K | 2 |
| PEOPLE'S BANK, | SRI LANKA | $100.0K | 2 |
| AUSTELL PHARMACEUTICALS ( PTY) LIMITED | SOUTH AFRICA | $100.0K | 2 |
| M/S. OOO JODAS EXPOIM.. | RUSSIA | $100.0K | 2 |
India's Teicoplanin is purchased by 108 buyers worldwide. The top buyer is SLIM PHARMACEUTICALS (PVT) LTD, (SRI LANKA), followed by YADEN INTERNATIONAL (PVT) LTD and MEDPRO PHARMACEUTICA PTY LTD.
Timeline: 12β18 months via Decentralized Procedure
GMP & Export Requirements
EU GMP (EudraLex Vol. 4); GMP certificate from EU competent authority; WHO Prequalification accepted as supporting evidence
Certificate of Pharmaceutical Product (CPP) from CDSCO; Written Confirmation for API export per EU requirements; EU FMD serialization mandatory
Note: Indian manufacturers must hold EU GMP certificate. EU Falsified Medicines Directive (FMD) serialization and tamper-evident packaging mandatory.
Regulatory information is provided for general reference based on publicly available guidelines. Requirements vary by formulation, dosage form, and therapeutic classification. Exporters should consult qualified regulatory affairs professionals for case-specific guidance.
| 9 | CELON LABORATORIES PRIVATE LIMITED | $82.4K | 6 | 1 | $13.7K |
Sanofi India Limited ranks #7 among 60 Indian Teicoplanin exporters. Average shipment value of $16.9K compared to the market average of $95.7K. The closest competitors by value are NEON LABORATORIES LIMITED and VENUS REMEDIES LIMITED.
Verify manufacturer licensing and export certifications with the official agencies above.
Government-Sourced Data
Official DGFT customs records
Transparent Methodology
Calculations fully disclosed above
Global Coverage
Exports to 44+ countries, 108+ buyers
Expert-Reviewed
Analyzed by pharmaceutical trade specialists
Access shipment-level records, pricing trends, and buyer contacts for Sanofi India Limited.
Request DemoView Pricing βTrade data sourced from Indian Customs (DGFT) export shipment records. Values represent FOB export value in USD. Market share calculated relative to total Indian pharmaceutical exports for Teicoplanin. For current shipment-level data, contact TransData Nexus.