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    Company profile for Zhejiang Hengkang Pharmaceutical

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    Hengkang Pharma invites global customers to join CPHI exhibition

    08 Oct 2024

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    CPHI Milan 2024 Zhejiang Hengkang Pharm

    24 Sep 2024

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    Kactus Biosystems and Hengkang Pharma reached a strategic cooperation

    22 May 2023

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    Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

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    About

    Established in 2004 and headquartered in Hangzhou, Hengkang established multiple factories, research and sales centers in Zhejiang, Shandong, and Henan. With facilities conforming to global API standards, along with professional R&D and marketing teams, Hengkang’s operations span major pharmaceutical markets such as China, Europe, the CIS region, Japan, and South Korea. Hengkang has established long-term and stable relationships with nearly 70 countries overseas and hundreds of domestic enterprises. Note: Product(s) under patent(s) are offered only for R&D purposes as per the Patent Act & not for commercial sale.

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    Zhejiang Hengkang PharmaceuticalChina Flag
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    China
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    11 Chengen Road, Pubagang Town, Sanmen County, Zhejiang Province, Zip code: 31...
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    +86 57683372028
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    marketing@hengkangpharm.cn
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    https://en.hengkangpharm.cn/
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    Product List 2026

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    GMP Certificate 2024

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    DATA COMPILATION #PharmaFlow

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    Chinese FDA-registered generic facilities gain steam, India maintains lead with 396 facilities

    Chinese FDA-registered generic facilities gain steam, India maintains lead with 396 facilities

    Every year, the US Food and Drug Administration (FDA) publishes the user fee amounts it will collect from manufacturers of pharmaceuticals, generic drugs, biosimilars and medical devices in the coming financial year. The fee for fiscal year 2025 under the Generic Drug User Fee Act (GDUFA) was published on July 31, 2024.The GDUFA, established in 2012, authorizes FDA to assess and collect fees from drug manufacturers to expedite the delivery of safe, high-quality, and affordable generic drugs to the American public.The FDA’s facility payments list under GDUFA reveals that as of November 14, 2024, 1,397 facilities had paid their registration fees for financial year 2025. Of these facilities, 707 or 50.6 percent are active pharmaceutical ingredients (API) facilities, 405 or 29 percent are finished dosage forms (FDF) facilities, 69 (4.9 percent) are facilities that produce both APIs and FDFs, and 216 (15.5 percent) are contract manufacturing services (CMO) sites.Teva Pharmaceuticals, with 29 facility registrations, led the list of companies, followed by Aurobindo Pharma, Sun Pharma, and Dr. Reddy's Laboratories. Fiscal year Facility Registrations 2016 1,425 2017 1,442 2018 1,269 2019 1,286 2020 1,300 2021 1,340 2022 1,385 2023 1,394 2024 1,447 2025 1,397  Generic Drug Facilities Registered with the US FDA for FY2025 (Free Excel Available)India continues to lead with 396 facilities, US and China follow India maintains its dominance in total facility registrations with the FDA, registering 396 facilities for FY2025. This includes 214 API facilities, 135 FDF facilities, 21 facilities engaged in both API and FDF activities, and 26 CMO facilities.The United States holds the second position with 328 facilities, while China strengthened its third position with 197 facilities.With 214 API facilities, India continues to have the largest share of API manufacturing sites, outmatching the combined total of China (128) and the US (83), which together account for 211 facilities. Among European manufacturers, Italy leads with 59 API manufacturing sites, followed by Spain (30) and Germany (25).The US has maintained its lead in FDF facilities with 143 sites, followed closely by India with 135 sites and China with 45 sites. Country API FDF Both CMO Total India 214 135 21 26 396 US 83 143 13 89 328 China 128 45 12 12 197 Italy 59 3 2 19 83 Germany 25 4 1 15 45 Spain 30 9 1 4 44 Canada 7 17   13 37 Taiwan 9 6 5 4 24 Switzerland 15 4   4 23 France 16     6 22 Japan 18   1   19 United Kingdom 12 1   2 15 Mexico 9 1   1 11 Ireland 5 5   1 11   Generic Drug Facilities Registered with the US FDA for FY2025 (Free Excel Available) GDUFA III user fee rates increase across categories for FY25The GDUFA, which was reauthorized on September 30, 2022 (as GDUFA III), continues with provisions that will last until September 30, 2027. In July 2024, the FDA published updated user fee rates for FY2025.The facility fees have seen increases across all categories. API facility fees increased by 3 percent for domestic sites (to US$ 41,580) and 2 percent for foreign sites (to US$ 56,580). FDF facility fees rose by 5 percent for both domestic (to US$ 231,952) and foreign sites (to US$ 246,952). CMO facility fees increased by 5 percent for domestic sites (to US$ 55,668) and 4 percent for foreign sites (to US$ 70,668).Additionally, the fee for large-, medium- and small-sized drug applicants has increased by over 9 percent, compared to the 7 percent increase seen in 2023. Generic Drug Facilities Registered with the US FDA for FY2025 (Free Excel Available) China leads new facility registrations as FDA records 41 new units in FY25Out of the total 1,397 facilities registered for FY2025, 41 were new registrations (going by Facility FDA Establishment Identifier numbers). China led the way with 13 new facilities, followed closely by India with 11 new facilities, while the US secured the third position with eight new facilities.The new registrations included 15 API facilities, 13 CMO facilities, 12 FDF facilities, and one facility engaged in both API and FDF activities. Chinese companies dominated the new FDF registrations with six facilities: Chengdu Shuode Pharma, Chengdu Suncadia Medicine, Cipla (Jiangsu), GE Healthcare (Shanghai), Luoxin Aurovitas Pharma (Chengdu), and Zhejiang Xianju Pharma.India added two new FDF facilities through Eugia Steriles and Zydus Pharma. Malaysia registered two FDF facilities through Novugen Pharma and Novugen Oncology, while Turkey’s Insud Pharma subsidiary Exeltis and US’ RK Pharma registered one FDF facility each.The 13 new CMO facilities included, Acme Generics, Emcure, Esjay Pharma, Fordoz Pharma, Fourrts Laboratories, Laboratoires KABS, PharmaMax, Quality Packaging Specialists International, Ritsa Pharma, Shanghai Aucyun Pharma, Sichuan Huiyu Pharma, Taejoon Pharm, and Tubilux Pharma.In the API category, the 15 new registrations included Acharya Chemicals, Hainan Poly Pharma, CBL Patras, EUROAPI, Hybio Pharma, Medilux Laboratories, Metrochem API, Purolite, Chengdu Easton Biopharma, Sionc Pharma, Smithfield Bioscience, Xttrium Laboratories, Zhejiang Hengkang Pharma, Moehs Iberica and Shilpa Pharma. Armstrong Pharmaceuticals registered the sole facility for both APIs and FDFs.So far, 92 facilities have not renewed their registration. Among these was a facility owned by Sandoz subsidiary Eon Labs in Wilson, North Carolina (US), which is permanently closed. In fact, the geographical distribution of non-renewals shows that 30 facilities were from the US, while India and China accounted for 14 and nine non-renewals respectively. Generic Drug Facilities Registered with the US FDA for FY2025 (Free Excel Available) Our viewThe FY 2025 GDUFA facility registration data indicates a continued strong presence of Indian manufacturers in the US generic drug market, particularly in API production. However, China's leadership in new facility registrations, especially in FDF manufacturing, suggests that the global generic drug supply chain landscape may evolve considerably in the coming years. 
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    NEWS #PharmaBuzz

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    Hengkang Pharma invites global customers to join CPHI exhibition
    Hengkang Pharma invites global customers to join CPHI exhibition

    08 Oct 2024

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    https://en.hengkangpharm.cn/index.php/news/cphi-milan-2024-zhejiang-hengkang-pharm/

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    08 Oct 2024
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    CPHI Milan 2024 Zhejiang Hengkang Pharm
    CPHI Milan 2024 Zhejiang Hengkang Pharm

    24 Sep 2024

    // PRESS RELEASE

    https://en.hengkangpharm.cn/index.php/news/cphi-milan-2024-zhejiang-hengkang-pharm/

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    24 Sep 2024
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    Kactus Biosystems and Hengkang Pharma reached a strategic cooperation
    Kactus Biosystems and Hengkang Pharma reached a strategic cooperation

    22 May 2023

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    http://hengkangpharm.cn/new_detail_en/id/8.html

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    22 May 2023
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    KaiKa Biotechnology and HengKang Reach Strategic Cooperation
    KaiKa Biotechnology and HengKang Reach Strategic Cooperation

    28 Feb 2023

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    http://hengkangpharm.cn/new_detail/id/18.html

    PRESS RELEASE
    28 Feb 2023
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    Zhejiang Hengkang Meiji Pharma to enter the field of green synthetic biology
    Zhejiang Hengkang Meiji Pharma to enter the field of green synthetic biology

    10 Jan 2023

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    http://hengkangpharm.cn/new_detail_en/id/6.html

    PRESS RELEASE
    10 Jan 2023
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    Vienna Tides EURO 2022 meet for Phosphoramidite for oligonucleotides
    Vienna Tides EURO 2022 meet for Phosphoramidite for oligonucleotides

    18 Nov 2022

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    http://hengkangpharm.cn/new_detail_en/id/3.html

    PRESS RELEASE
    18 Nov 2022
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    ALL APIs

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    01

    Mesalazine

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF arrow-down Click Us! arrow-down
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    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2022-10-20

    Pay. Date : 2022-09-16

    DMF Number : 37319

    Submission : 2022-08-17

    Status : Active

    Type : II

     CEP/COS arrow-down
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    Certificate Number : CEP 2021-400 - Rev 01

    Issue Date : 2025-12-10

    Type : Chemical

    Substance Number : 1699

    Status : Valid

     JDMF arrow-down
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    Registration Number : 305MF10102

    Registrant's Address : No. 11 Chengen Road, Pubagan Town, Sanmen, Zhejiang, China

    Initial Date of Registration : 2023-08-30

    Latest Date of Registration :

    EU-WCInactive-api
    ✖

    Date of Issue : 2022-04-28

    Valid Till : 2024-12-15

    Written Confirmation Number : ZJ220039

    Address of the Firm :

    NDC KDMF VMF BR arrow-down
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    Available Reg. Filing : BR
    AUDIT
    Zhejiang Hengkang Pharmaceutical

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    02

    Deferasirox

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 41051

    Submission : 2024-12-31

    Status : Active

    Type : II

     CEP/COS arrow-down
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    Certificate Number : CEP 2024-292 - Rev 00

    Issue Date : 2024-12-18

    Type : Chemical

    Substance Number : 2933

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Others AUDIT
    Zhejiang Hengkang Pharmaceutical

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    03

    Mesalazine

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
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    Certificate Number : R1-CEP 2015-209 - Rev 00

    Issue Date : 2021-05-06

    Type : Chemical

    Substance Number : 1699

    Status : Valid

     JDMF arrow-down
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    Registration Number : 227MF10271

    Registrant's Address : No. 1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China

    Initial Date of Registration : 2015-12-01

    Latest Date of Registration :

    EU-WC NDC KDMF VMF BR arrow-down
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    Available Reg. Filing : BR
    AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
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    04

    Acemetacin

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : R0-CEP 2022-226 - Rev 00

    Issue Date : 2022-11-10

    Type : Chemical

    Substance Number : 1686

    Status : Valid

     JDMF EU-WCInactive-api
    ✖

    Date of Issue : 2023-01-18

    Valid Till : 2026-01-17

    Written Confirmation Number : ZJ230010

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
    Zhejiang Hengkang Pharmaceutical

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    05

    Amiodarone Hydrochloride

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2021-349 - Rev 01

    Issue Date : 2025-09-05

    Type : Chemical

    Substance Number : 803

    Status : Valid

     JDMF EU-WCInactive-api
    ✖

    Date of Issue : 2022-11-11

    Valid Till : 2024-12-15

    Written Confirmation Number : ZJ220038

    Address of the Firm :

    NDC KDMF arrow-down
    ✖

    Registrant Name : Bansen Co., Ltd.

    Registration Date : 2025-06-17

    Registration Number : 20250617-210-J-1911

    Manufacturer Name : Zhejiang Hengkang Pharmaceutical Co., Ltd.

    Manufacturer Address : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China

     VMF BR, RU arrow-down
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    Available Reg. Filing : BR, RU
    AUDIT
    Zhejiang Hengkang Pharmaceutical

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    06

    Benserazide Hydrochloride

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2022-310 - Rev 01

    Issue Date : 2023-12-11

    Type : Chemical

    Substance Number : 1173

    Status : Valid

     JDMF EU-WCInactive-api
    ✖

    Date of Issue : 2023-04-11

    Valid Till : 2026-01-26

    Written Confirmation Number : ZJ230055

    Address of the Firm :

    NDC KDMF arrow-down
    ✖

    Registrant Name : Samoh Pharmaceutical Co., Ltd.

    Registration Date : 2025-03-05

    Registration Number : 20250305-211-J-1544

    Manufacturer Name : Zhejiang Hengkang Pharmaceutical Co., Ltd.

    Manufacturer Address : No. 11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China

     VMF Others AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
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    Market
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    07

    Benserazide Hydrochloride

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : R0-CEP 2018-183 - Rev 00

    Issue Date : 2021-09-27

    Type : Chemical

    Substance Number : 1173

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Others AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    08

    Eltrombopag

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 40357

    Submission : 2024-11-25

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    09

    Tenoxicam

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2011-331 - Rev 02

    Issue Date : 2019-11-18

    Type : Chemical

    Substance Number : 1156

    Status : Valid

     JDMF EU-WC NDC KDMF VMF RU arrow-down
    ✖
    Available Reg. Filing : RU
    AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    10

    Vonoprazan Fumarate

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 40356

    Submission : 2024-12-29

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF BR arrow-down
    ✖
    Available Reg. Filing : BR
    AUDIT
    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

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    CEP/COS

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    01

    Acemetacin, Pubagang site

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : R0-CEP 2022-226 - Rev 00

    Status : Valid

    Issue Date : 2022-11-10

    Type : Chemical

    Substance Number : 1686

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    02

    Amiodarone hydrochloride

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : R1-CEP 2007-187 - Rev 04

    Status : Withdrawn by Holder

    Issue Date : 2019-12-12

    Type : Chemical

    Substance Number : 803

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

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    03

    Amiodarone hydrochloride, Pubagang site

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : CEP 2021-349 - Rev 01

    Status : Valid

    Issue Date : 2025-09-05

    Type : Chemical

    Substance Number : 803

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    04

    Benserazide hydrochloride

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : R0-CEP 2018-183 - Rev 00

    Status : Valid

    Issue Date : 2021-09-27

    Type : Chemical

    Substance Number : 1173

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    05

    Benserazide hydrochloride, Pubagang site

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : CEP 2022-310 - Rev 01

    Status : Valid

    Issue Date : 2023-12-11

    Type : Chemical

    Substance Number : 1173

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    06

    Deferasirox

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : CEP 2024-292 - Rev 00

    Status : Valid

    Issue Date : 2024-12-18

    Type : Chemical

    Substance Number : 2933

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

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    Market
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    07

    Mesalazine, HP

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : R1-CEP 2015-209 - Rev 00

    Status : Valid

    Issue Date : 2021-05-06

    Type : Chemical

    Substance Number : 1699

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    08

    Mesalazine, Pubagang site

    China
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    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : CEP 2021-400 - Rev 01

    Status : Valid

    Issue Date : 2025-12-10

    Type : Chemical

    Substance Number : 1699

    Zhejiang Hengkang Pharmaceutical

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    Market
    Place

    09

    Tenoxicam

    China
    arrow
    CPhI Japan
    Booth #2A46
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothZhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

    Zhejiang Hengkang Pharmaceutical

    Certificate Numbers : R1-CEP 2011-331 - Rev 02

    Status : Valid

    Issue Date : 2019-11-18

    Type : Chemical

    Substance Number : 1156

    Zhejiang Hengkang Pharmaceutical

    Product
    Web Link

    Stock Recap
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    Contact Zhejiang Hengkang Pharmaceutical and get a quotation

    Zhejiang Hengkang Pharmaceutical is a supplier offers 59 products (APIs, Excipients or Intermediates).

    Find a price of Mesalazine bulk with DMF, CEP, JDMF offered by Zhejiang Hengkang Pharmaceutical

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