Tablets
Film-coated, chewable and effervescent tablets across anti-infective, cardiovascular and GI therapy areas.
107 productsBLISTER & BOTTLE
CHINA GMP CERTIFIED MANUFACTURER
Generic pharmaceuticals,
Generic pharmaceuticals,
manufactured to GMP standards
for 40+ markets.
Feiyue Pharma is an integrated manufacturer in Ningbo, China, supplying 359 registered generic products — injectables, tablets, capsules, infusions and oral liquids — to distributors, hospitals and tender authorities worldwide.
CoPP / CoA on every batchCTD & ACTD dossiersRegistration support included
359
Registered products
6
Dosage forms produced
40+
Countries supplied
PRODUCT RANGESix dosage forms,
Six dosage forms,
one production campus.
Every product is manufactured, packed and released in-house under Chinese GMP. Full documentation — CoPP, CoA, batch records and stability data — is issued with each shipment.
Capsules
Hard gelatin capsules for antibacterials and combination therapies, blister or bottle pack.
28 products250–500 MG
Small-Volume Injectables
Ampoules and vials covering antibacterials, analgesics, anaesthetics, PPIs, vitamins and antiemetics.
90 productsAMP & VIAL
Powder for Injection
Cephalosporins, carbapenems, penicillins and β-lactamase inhibitor combinations in dedicated segregated lines.
92 productsSEGREGATED LINE
Large-Volume Infusion
Glass bottles and flexible bags for IV solutions, amino acids and combined infusion products.
35 productsGLASS & BAG
Other Oral Preparations
Dry suspensions, granules and oral rehydration salts supplied in retail and clinical pack sizes.
7 productsSUSPENSION
MANUFACTURINGOne site, end to end —
One site, end to end —
from dispensing to release.
Nothing is outsourced. API dispensing, formulation, filling, terminal sterilisation, packing and quality release all happen inside our campus in Ningbo, which is why we can commit to documentation and lead times we fully control.
Aseptic filling lines for small-volume injectables with terminal sterilisation capability
Dedicated β-lactam facilities physically separated from non-β-lactam production to prevent cross-contamination
Oral solids capacity across blister, strip and bottle pack formats including Alu-Alu and PVC
Large-volume parenterals in glass bottles and flexible bags with validated terminal sterilisation
In-process and finished-product QC with retained samples and full batch traceability
QUALITY & REGISTRATIONThe paperwork is part
The paperwork is part
of the product.
A supply that cannot be registered is not a supply. Our regulatory team prepares dossiers in the format your authority requires, and fronts the technical answers during assessment.
MODULE 1–5CTD DossiersCompiled to ICH CTD structure — administrative, quality, non-clinical and clinical modules ready for submission.
ASEAN FORMATACTD DossiersFull Part I–IV ACTD sets prepared for ASEAN and national authorities that follow the ASEAN Common Technical Dossier.
BATCH RELEASECoPP & CoACertificate of Pharmaceutical Product and batch-specific Certificate of Analysis issued with every shipment.
FREE SALEFSC SupportCertificate of Free Sale documentation coordinated alongside the dossier for your registration file.
STABILITYOngoing DataReal-time and accelerated stability data maintained per ICH climatic zone requirements for your market.
DMF / OPEN PARTAPI Source FilesOpen and closed parts of the active substance master file provided where the authority requires it.
HOW IT WORKSFrom enquiry to
From enquiry to
first shipment.
01
Product shortlist
Send the molecules and strengths you need. We confirm availability, registration status in your market and minimum order quantity.
02
Quotation & samples
Commercial offer within 48 hours, with reference samples and specifications shipped for evaluation.
03
Dossier transfer
CTD or ACTD set prepared in English, translated into Spanish where required, handed to your regulatory team.
04
Production & release
Order manufactured under GMP, batch tested, released with CoA and delivered with full export documentation.
EXPORT MARKETSRegistrations held and submissions in progress
Registrations held and submissions in progress
across 40+ countries.
We have supported dossier submissions and repeat shipments in Latin America, the Middle East, South and Southeast Asia and Africa — including Spanish-language submissions.
Costa RicaPakistanIraqYemenSaudi ArabiaPhilippinesVietnamPeruNigeriaDominican RepublicGuatemalaBolivia+ 28 more countries
359
Registered generic products across six dosage forms
6
Dosage forms manufactured in-house
48h
Typical turnaround for a commercial quotation
100%
Batches released against specification with CoA
Tell us which molecules you need.
We will come back with availability and price.
Send the product list, strengths and target market. You will get a commercial offer within 48 hours — including the registration documents we can support for your country.