Gefitinib — Manufacturers, Suppliers & Wholesale Price in India
Oncology API (EGFR inhibitor). Prescription product — documentation required.
Wholesale price
Price on request
Quoted per quantity, grade and destination. State a target price to get faster, more serious responses.
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- Matched to up to 5 suppliers
- We never take a commission
Gefitinib (CAS 184475-35-2) is a tyrosine-kinase inhibitor used in targeted oncology therapy for EGFR-mutated non-small cell lung cancer. India is a significant producer of gefitinib API, supplying generic manufacturers and authorised importers in markets where the molecule is off-patent or licensed, alongside regulated markets under DMF-supported supply.
Technical specification
| Grade | In-house / export standard (pharmacopoeial monographs where applicable) |
| CAS No. | 184475-35-2 |
| Assay (dried basis) | ≥ 99.0% (per manufacturer spec) |
| Appearance | White to off-white powder |
| Impurity profile | Nitrosamine risk assessment and impurity data per batch available from established manufacturers |
| Packing | 1–5 kg aluminium tin with PE liner / per buyer spec |
| MOQ | Typically 1–25 kg |
Manufacture of gefitinib tablets (250 mg standard) by licensed generic manufacturers and formulation exporters. Buyers must hold the applicable manufacturing or import authorisations in their jurisdiction — TradeBioIndia verifies importer status before routing multi-seller enquiries.
Small-volume specialist packing: 1–5 kg sealed aluminium tins with PE liners, tamper-evident, per buyer requirement. Cold-chain not typically required; controlled-temperature storage applies. Documentation: batch COA with impurity profile, MSDS, GMP certificate, Certificate of Origin, and export licences as applicable to destination-country rules.
Documents suppliers provide
- Certificate of Analysis (COA) for every batch
- Material Safety Data Sheet (MSDS)
- GMP certificate and manufacturing licence
- Free sale certificate for export markets, issued on request
- DMF / regulatory filing status, where the supplier holds one
- Origin, packing list and commercial invoice for the shipment
What we do not do
TradeBioIndia does not test, store, ship or certify any product, and does not verify every document a supplier provides. Buyers must independently validate licences, certificates and product suitability before contracting — especially for prescription products.
Scheduled product handling
Gefitinib is a prescription (Scheduled) product. Enquiries routed to multiple suppliers require verified importer or distributor documentation. Listings may not offer this product to unlicensed buyers, and prohibited items cannot be listed at all.
Who can buy gefitinib API through TradeBioIndia?
Licensed pharmaceutical manufacturers, authorised importers and licensed distributors. Multi-seller enquiry blasts require verified importer or distributor documentation; direct enquiries to a single seller remain open.
What MOQ applies to oncology APIs?
Typically 1–25 kg — oncology APIs trade in small, high-value volumes compared with commodity APIs.
Do suppliers provide nitrosamine risk assessments?
Established Indian manufacturers provide nitrosamine risk evaluation and impurity-profile data per batch — request it explicitly in the enquiry.
What documentation is needed for export?
COA, MSDS, GMP certificate and Certificate of Origin as standard; destination-country import and controlled-substance-adjacent rules apply and are the buyer's responsibility to satisfy. TradeBioIndia is a listing platform and is not a party to any transaction between buyer and supplier.
Suppliers for Gefitinib
4 companies currently listing in Oncology. Send your requirement straight to one of them, or to all of them — there is no limit and no fee.
Or let the desk handle it
Unaddressed requirements go to the pool, where we route them to the best-matched suppliers for the category, certification, capacity and region — and record why.