Shandong Chenghui Shuangda Pharmaceutical
About Shandong Chenghui Shuangda Pharmaceutical
Certifications
Categories
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Country/Region:China
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On CPHI since:2023
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Certificates:4
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Employees:500 - 999
Company types
Primary activities
Products from Shandong Chenghui Shuangda Pharmaceutical (3)
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Product Dapagliflozin
Product name: Dapagliflozin propanediol monohydrateSynonyms: (2S,3R,4R,5S,6R)-2-(4-CHLORO-3-(4-ETHOXYBENZYL)PHENYL)-6-(HYDROXYMETHYL)TETRAHYDRO-2H-PYRAN-3,4,5-TRIOLCOMPOUNDWITH(S)-POPANE-1,2,3,4,5-(HYDROXYMETHYL)TETRAHYDRO PROPANE-1,2-DIOL(1:1)HYDRATE;BMS512148(2S)-1,2-propanediol;CS-1307;Dapaglifloz... -
Product Finerenone
Product name: Finerenone
Alias: Finerenone (BAY94-8862); (4S)-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide; (4S)-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide; BAY94-8862; BAY948862; 1,6-Naphthyridine-3-... -
Product Letermovir
Product name: Letermovir
alias: Letemovir; Lemovir; Letemovir; (S)-2-(8-fluoro-3-(2-methoxy-5-(trifluoromethyl)phenyl)-2-(4-(3-methoxyphenyl)piperazin-1-yl)-3,4-dihydroquinazolin-4-yl)acetic acid; Letemovir Standard 005; Letemovir; Letemovir-letemovir; Letemovir-letemovir Letermovir
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Shandong Chenghui Shuangda Pharmaceutical Resources (2)
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News Tetracaine HCl API Granted CEP by EDQM
We are proud to announce that our pharmaceutical ingredient Tetracaine Hydrochloride has been granted the Certificate of Suitability to the European Pharmacopoeia (CEP) by the European Directorate for the Quality of Medicines (EDQM) on August 20, 2025. This marks a significant milestone as we become the first company in China and one of only three global manufacturers to hold this certification for this critical local anesthetic.
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Brochure About us
Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. specializes in R&D and production of APIs and advanced intermediates , CDMO/CRO/OEM, and Technology Transfer of Finished Formulations. With 23 years of production experience, the company operates 6 GMP-compliant workshops, achieving a monthly capacity of 100 tons to meet cGMP requirements. Currently, the factory has registered 21 APIs in NMPA, filed 4 US-DMFs, and applied for 9 CEPs, while successfully passing audits by MFDS, US FDA, and global customers.


