Symbiotec Pharmalab DMF, CEP, Written Confirmations, FDF, Prices, Patents, Patents & Exclusivities, Dossier, Manufacturer, Licensing, Distributer, Suppliers, News, GMP

Symbiotec Pharmalab plans IPO to boost specialty pharma market

25 Jun 2025

// PRESS RELEASE

Symbiotec eyes IPO to give exit to PE investors

17 Oct 2024

// VCCIRCLE

Lilly to Construct $5B Manufacturing Facility in Virginia

17 Sep 2025

// REUTERS

DATA COMPILATION
#PharmaFlow

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CPhI WW Frankfurt

Booth #12.1D45

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DIGITAL CONTENT

6 Corporate Content #SupplierSpotlight, 1 Data Compilation #PharmaFlow, 2 News #PharmaBuzz

media
6 Corporate Content #SupplierSpotlight
1 Data Compilation #PharmaFlow
2 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

242 All APIs, 42 USDMF, 22 CEP/COS, 1 JDMF, 197 EU WC, 20 KDMF, 52 NDC API, 85 Listed APIs

242 All APIs
42 USDMF
22 CEP/COS
1 JDMF
197 EU WC
20 KDMF
52 NDC API
85 Listed APIs

INTERMEDIATES

5 All Intermediates

5 All Intermediates

KEY PRODUCTS

16-Alpha-Hydroxy Prednisolone, Beclomethasone Dipropionate, Betamethasone, Betamethasone Acetate, Betamethasone Dipropionate, Betamethasone Sodium Phosphate, Betamethasone Valerate, Clascoterone, Clobetasol Butyrate, Clobetasol Propionate, Conjugated Estrogens, Deflazacort, Desoximetasone, Dexamethasone, Dexamethasone Sodium Phosphate, DHA, Estradiol, Estradiol Acetate, Estradiol Benzoate, Estradiol Cypionate, Estradiol Enanthate, Estradiol Valerate, Estrone, Ethinyl Estradiol, Flumethasone, Flumethasone Pivalate, Fluorometholone, Fluorometholone Acetate, Hydrocortisone, Hydrocortisone Acetate, Hydrocortisone Butyrate, Hydrocortisone Sodium Succinate, Hydrocortisone Valerate, Hydroxyprogesterone Caproate, Methylprednisolone, Methylprednisolone Aceponate, Methylprednisolone Acetate, Methylprednisolone Hemisuccinate, Methylprednisolone Sodium Succinate, Mometasone Furoate, Norethisterone, Norethisterone Acetate, Norethisterone Enanthate, Prasterone, Prasterone Acetate, Prednisolone, Prednisolone Acetate, Prednisolone Sodium Metasulfobenzoate, Prednisolone Sodium Phosphate, Prednisolone Valerate Acetate, Progesterone, Serratiopeptidase, Teicoplanin, Testosterone, Testosterone Cypionate, Testosterone Enanthate, Testosterone Propionate, Testosterone Undecanoate, Vancomycin Hydrochloride

16-Alpha-Hydroxy Prednisolone
Beclomethasone Dipropionate
Betamethasone
Betamethasone Acetate
Betamethasone Dipropionate
Betamethasone Sodium Phosphate
Betamethasone Valerate
Clascoterone
Clobetasol Butyrate
Clobetasol Propionate
Conjugated Estrogens
Deflazacort
Desoximetasone
Dexamethasone
Dexamethasone Sodium Phosphate
DHA
Estradiol
Estradiol Acetate
Estradiol Benzoate
Estradiol Cypionate
Estradiol Enanthate
Estradiol Valerate
Estrone
Ethinyl Estradiol
Flumethasone
Flumethasone Pivalate
Fluorometholone
Fluorometholone Acetate
Hydrocortisone
Hydrocortisone Acetate
Hydrocortisone Butyrate
Hydrocortisone Sodium Succinate
Hydrocortisone Valerate
Hydroxyprogesterone Caproate
Methylprednisolone
Methylprednisolone Aceponate
Methylprednisolone Acetate
Methylprednisolone Hemisuccinate
Methylprednisolone Sodium Succinate
Mometasone Furoate
Norethisterone
Norethisterone Acetate
Norethisterone Enanthate
Prasterone
Prasterone Acetate
Prednisolone
Prednisolone Acetate
Prednisolone Sodium Metasulfobenzoate
Prednisolone Sodium Phosphate
Prednisolone Valerate Acetate
Progesterone
Serratiopeptidase
Teicoplanin
Testosterone
Testosterone Cypionate
Testosterone Enanthate
Testosterone Propionate
Testosterone Undecanoate
Vancomycin Hydrochloride

SERVICES

API Manufacturing

pharmaServices
API Manufacturing
- 1 Biologics, Bioprocess & Fermentation

REF. STANDARDS & IMPURITIES

1 Others

otherProducts
1 Others

INSPECTIONS & REGISTRATIONS

16 FDA, 2 EDQM, 2 WHO-GMP, 2 GDUFA

inspections
16 FDA
2 EDQM
2 WHO-GMP
2 GDUFA

Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

About

Symbiotec, a leading API manufacturing company based in Indore, Central India, specializes in Cortico-Steroids and Steroid-Hormone APIs. Since 1995, their focus on R&D, sustainable operations, and innovation has driven their commitment to improving global healthcare access. With a state-of-the-art manufacturing facility inaugurated in 2004, Symbiotec has become a trusted provider in the industry. Their certifications including WHO-GMP, ISO, US FDA, and EU GMP showcase their dedication to quality and excellence. Over two decades, they've maintained their position through adaptability, efficiency, and competitive pricing.

CPhI WW FrankfurtCPhI WW Frankfurt

Industry Trade Show

Booth #12.1D45

28-30 October, 2025

Frankfurt
CPhI IndiaCPhI India

Industry Trade Show

Exhibiting

25-27 November, 2025

India Expo Centre, Greater Noida
SCI Medicinal Chemistr...SCI Medicinal Chemistry

Industry Trade Show

Not Confirmed

14-17 September, 2025

Cambridge, UK

CONTACT DETAILS

Click the arrow to open the dropdown

Country

India

Address

385, Pigdamber, Rau, Indore, MP, 453331

Telephone

+91 7316676405

symbiotec@symbiotec.in

Website

https://www.symbiotec.in/

https://www.linkedin.com/company/symbiotec-pharmalab-pvt-ltd-/

YouTube

Digital content

Explore the latest content creation from this company

CORPORATE CONTENT #SupplierSpotlight

Product List 2025

Open PDF

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API Product List 2025

Open PDF

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Intermediates Product List 2025

Open PDF

Upload

Products Under Development 2025

GMP Certificate 2024

Regulatory Filing

DATA COMPILATION #PharmaFlow

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.