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    Synthokem Labs Pvt Ltd is a privately owned company established in 1978, specializing in the production of Active Pharmaceutical Ingredients and Drug Intermediates. Operating across two states, Telangana and Andhra Pradesh, in India, the company has earned global recognition for its expertise in manufacturing and distributing a diverse range of products. With a strong focus on research and development, Synthokem Labs is dedicated to offering accessible and affordable pharmaceutical solutions to those in need.

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    B-5 Industrial Estate, Sanathnagar, Hyderabad 500018, Telangana
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    +91 4023702061
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    Product List 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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    ALL APIs

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    01

    Guaifenesin

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2014-04-08

    Pay. Date : 2013-09-12

    DMF Number : 10413

    Submission : 1993-08-13

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2019-065 - Rev 01

    Issue Date : 2025-01-15

    Type : Chemical

    Substance Number : 615

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC arrow-down
    ✖

    NDC Package Code : 58343-0130

    Start Marketing Date : 2013-11-01

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF arrow-down
    ✖

    Registrant Name : Aging Life Science Co., Ltd.

    Registration Date : 2025-12-15

    Registration Number : 20251215-211-J-2076

    Manufacturer Name : Synthokem Labs Private Ltd.

    Manufacturer Address : Unit-Ⅱ Plot No. 222 to 224 & 235 to 237 Phase-Ⅱ, IDA, Pashamylaram Patancheru Mandal, Sangareddy District, Telangana State, India.

     VMF Others AUDIT arrow-down
    Synthokem Labs

    02

    Mebeverine

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2021-271 - Rev 00

    Issue Date : 2023-09-25

    Type : Chemical

    Substance Number : 2097

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    03

    Methocarbamol

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2013-10-04

    Pay. Date : 2013-09-30

    DMF Number : 10410

    Submission : 1993-08-13

    Status : Active

    Type : II

     CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC arrow-down
    ✖

    NDC Package Code : 58343-0138

    Start Marketing Date : 1983-01-01

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF arrow-down
    ✖

    Registrant Name : Daeshin Pharmaceutical Co., Ltd.

    Registration Date : 2013-08-28

    Registration Number : 20130828-81-D-115-04

    Manufacturer Name : Synthokem Labs Private Limited

    Manufacturer Address : B-5, Industrial Estate, Sanathnagar - 500 018, Hyderabad, Telangana State, India

     VMF Others AUDIT arrow-down
    Synthokem Labs

    04

    Prazosin Hydrochloride

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 39220

    Submission : 2024-01-03

    Status : Active

    Type : II

     CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC arrow-down
    ✖

    NDC Package Code : 58343-0140

    Start Marketing Date : 2022-10-28

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    05

    Chlorphenesin

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-02-10

    Valid Till : 2028-02-09

    Written Confirmation Number : WC-0603

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    06

    Drotaverine

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-02-10

    Valid Till : 2028-02-09

    Written Confirmation Number : WC-0603

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    07

    Guaifenesin

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS Inactive-api
    ✖

    Certificate Number : R1-CEP 1999-088 - Rev 05

    Issue Date : 2018-06-26

    Type : Chemical

    Substance Number : 615

    Status : Withdrawn by Holder

     JDMF EU-WCInactive-api
    ✖

    Date of Issue : 2022-07-07

    Valid Till : 2025-07-21

    Written Confirmation Number : WC-0020n

    Address of the Firm :

    NDC arrow-down
    ✖

    NDC Package Code : 58343-0132

    Start Marketing Date : 2012-11-11

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    08

    Mephenesin

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    09

    Mephenesin

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-02-10

    Valid Till : 2028-02-09

    Written Confirmation Number : WC-0603

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs

    10

    Sulfogaiacol

    India

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

    arrow
    BePharma
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothSynthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
    USDMF CEP/COS JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-25

    Valid Till : 2028-07-14

    Written Confirmation Number : WC-0358

    Address of the Firm :

    NDC KDMF VMF Others AUDIT arrow-down
    Synthokem Labs
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    REF. STANDARDS & IMPURITIES

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    ABOUT THIS PAGE

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    Synthokem Labs is a supplier offers 12 products (APIs, Excipients or Intermediates).

    Find a price of Guaifenesin bulk with DMF, CEP, WC offered by Synthokem Labs

    Find a price of Mebeverine bulk with CEP, WC offered by Synthokem Labs

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    Find a price of Prazosin Hydrochloride bulk with DMF, WC offered by Synthokem Labs

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