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Company directoryChina company filings

Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized

Check drug filings and source records for this company-name string.

Listed by the company name as recorded in the source, without merging affiliated entities.

Page reference 23eebaa3b4

Complete CDE snapshot
2026/11/13 06:42
Matching scope
Loaded public-source records only

These counts cover loaded acceptance records only. First-applicant and co-applicant counts are not added together. CDE data as of 2026/11/13 06:42.

Drug filings

13 acceptance records as first applicant, grouped into 8 source drug names. Source data as of 2026/11/13 06:42.

Acceptance records are de-duplicated by acceptance number. Drug names are normalized only for width and whitespace; dosage forms and combinations remain separate. Application types are retained from the source. Expand a drug to inspect each record. Published drugs link to their drug pages; other names do not create new public drug pages.

Acetylcysteine Tablets 2 records · Latest accepted 2026/10/13

Generic · 2

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2602506Generic2026/10/13Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
CYHS2502008Generic2025/06/06Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Baricitinib Tablets 1 records · Latest accepted 2026/02/27

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2600566Generic2026/02/27Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Lactulose Oral Solution 3 records · Latest accepted 2025/12/11

Generic · 3

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2504252Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
CYHS2504251Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
CYHS2504250Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
Glucosamine Sulfate Capsules 1 records · Latest accepted 2025/07/23

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2502668Generic2025/07/23Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Jiangsu Cheng Kang Pharma Co., Ltd. romanizedCDE ↗
Empagliflozin Tablets 2 records · Latest accepted 2025/07/08

Generic · 2

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2502413Generic2025/07/08Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
CYHS2502412Generic2025/07/08Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Roxadustat Capsules 1 records · Latest accepted 2025/06/12

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHB2501181Supplement2025/06/12Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Jiangsu Cheng Kang Pharma Co., Ltd. romanizedCDE ↗
Letermovir Tablets 1 records · Latest accepted 2025/04/22

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2501514Generic2025/04/22Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Edoxaban Tosilate Tablets 2 records · Latest accepted 2025/03/15

Generic · 2

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2501082Generic2025/03/15Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Shanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
CYHS2501081Generic2025/03/15Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Shanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗

Changes in the last 90 days

1 events from 2026/08/16 to 2026/11/13. CDE data as of 2026/11/13 06:42; NMPA data as of 2026/11/12 18:32.

This source was last successfully updated at 2026/11/12 18:32; current coverage may be incomplete.

Last 90 days, ordered by fact date. Marketing approvals, trial registrations, supplements, notices and review changes are labelled separately. Fact dates are approval dates, acceptance dates, trial first-publication dates or complete-snapshot observation dates, as applicable. Publication and site-observation dates are separate. Historical backfills are not current-period new events. Exit records cover currently inactive applications with an identifiable complete snapshot, not a full review history.

Accepted: 1 application

  1. 2026/10/13Accepted

    Acetylcysteine Tablets

    CYHS2602506

    Fact date: 2026/10/13 · Site observation date: 2026/10/22

    View source ↗

Under review

7 acceptance numbers with this company as first applicant are currently listed as under review by CDE. Source data as of 2026/11/13 06:42.

Under review
Drug Acceptance numberApplication typeAcceptedCompany / applicantView source
Acetylcysteine Tablets CYHS2602506Generic2026/10/13Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Baricitinib Tablets CYHS2600566Generic2026/02/27Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Lactulose Oral Solution CYHS2504252Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
Lactulose Oral Solution CYHS2504251Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
Lactulose Oral Solution CYHS2504250Generic2025/12/11Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized; Chi Feng Yuan Sheng Pharma Co., Ltd. romanizedCDE ↗
Empagliflozin Tablets CYHS2502413Generic2025/07/08Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗
Empagliflozin Tablets CYHS2502412Generic2025/07/08Jiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedCDE ↗

Catalogue holder records

5 loaded active catalogue records whose holder name matches this source company name. Source data as of 2026/11/13 06:39. Manufacturer-only records are excluded.

DrugMarketing authorization holderManufacturerApproval numberApprovedCatalogue category (source text)View source
Letermovir TabletsJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized国药准字H202655472026/08/04Generic approved under the new chemical-drug registration classificationCDE ↗
Glucosamine Sulfate CapsulesJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedJiangsu Cheng Kang Pharma Co., Ltd. romanized国药准字H202653112026/07/21Generic approved under the new chemical-drug registration classificationCDE ↗
Edoxaban Tosilate TabletsJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedShanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized国药准字H202650792026/07/08Generic approved under the new chemical-drug registration classificationCDE ↗
Edoxaban Tosilate TabletsJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedShanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized国药准字H202650982026/07/08Generic approved under the new chemical-drug registration classificationCDE ↗
Roxadustat CapsulesJiangxi Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedJiangsu Cheng Kang Pharma Co., Ltd. romanized国药准字H202640342026/04/14Generic approved under the new chemical-drug registration classificationCDE ↗

Only active catalogue records matching the source holder name are listed. A manufacturer role does not count as a holder record. The catalogue covers only part of the chemical-drug market; source categories do not establish complete market coverage or qualifications.

API registrations

0 loaded active API registrations whose first registered company matches this source company name. Source data as of 2026/11/13 06:41.

NameCompany / applicantRegistration numberStatusSource update dateView source
No matching records were found in the currently loaded source data; coverage dates are listed below.

Only loaded active API registrations not listed as cancelled are shown. A/I are source registration statuses. Records are listed by registration number and do not establish capacity or supply. The register does not identify the associated formulation.

Co-applicant records

0 acceptance records name this company after the first applicant. They are listed separately and are not included in first-applicant drug or filing counts. Source data as of 2026/11/13 06:42.

Co-applicant records
Drug Acceptance numberApplication typeAcceptedCompany / applicantView source
No matching records were found in the currently loaded source data; coverage dates are listed below.

How current is each source?

CDE acceptances and review
Last successful update: 2026/11/13 06:42
Chemical-drug catalogue
Last successful update: 2026/11/13 06:39
Full API register
Last successful update: 2026/11/13 06:41
NMPA drug delivery notices
Last successful update: 2026/11/12 18:32 · Current coverage may be incomplete

First index-page publication dates: 2026-10-29 to 2026-11-13; 2 pages pending. Covers loaded notices only, not a complete historical approval database.

Listed by the company name as recorded in the source, without merging affiliated entities.

This page summarizes loaded records only, without new source queries or collection. Parent companies, subsidiaries, former names and aliases are not merged. Counts from different sources must not be added together. No loaded record does not establish the absence of a filing or registration. Check original records where coverage is incomplete, an update has failed, or a source lies outside the loaded scope.

Fact dates are approval dates, acceptance dates, trial first-publication dates or complete-snapshot observation dates, as applicable. Publication and site-observation dates are separate. Historical backfills are not current-period new events. Exit records cover currently inactive applications with an identifiable complete snapshot, not a full review history.

Drugs with a verified official English name use that name only. Other drug names retain the Chinese source name marked No verified English name; names with a Chinese public page link to that page. Company labels use verified official names, Latin source names, then fixed-rule transliterations marked romanized; Chinese company names are not displayed. Marked unverified drug names and original statutory reference numbers may appear in Chinese.

Legal reference identifiers are retained verbatim. Company labels use official English entries where available, or a visibly marked fixed romanization. Unverified drug names retain the Chinese source name with a No verified English name marker. Other Chinese free text is not displayed; use the source links or source-name columns in CSV exports.