Hunan Sheng Xiang Zhong Pharmaceutical 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 1b8dcb9e5b
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
12 acceptance records as first applicant, grouped into 9 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.
玉竹膏 · No verified English name 1 records · Latest accepted 2025/12/02
Supplement · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYZB2502817 | Supplement | 2025/12/02 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
Oxcarbazepine Tablets 2 records · Latest accepted 2024/12/04
Generic · 2
Sodium Valproate Oral Solution 2 records · Latest accepted 2024/11/01
Generic · 2
丙戊酸钠糖浆 · No verified English name 2 records · Latest accepted 2024/02/19
Supplement · 2
Vortioxetine Hydrobromide Tablets 1 records · Latest accepted 2023/12/15
Generic · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYHS2303482 | Generic | 2023/12/15 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
Fluvoxamine Maleate Tablets 1 records · Latest accepted 2023/11/07
Generic · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYHS2303021 | Generic | 2023/11/07 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
Sodium Valproate Sustained-release Tablets(I) 1 records · Latest accepted 2023/10/24
Generic · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYHS2302854 | Generic | 2023/10/24 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
Levetiracetam Oral Solution 1 records · Latest accepted 2023/10/24
Generic · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYHS2302859 | Generic | 2023/10/24 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
布南色林片 · No verified English name 1 records · Latest accepted 2022/11/15
Generic · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| CYHS2201983 | Generic | 2022/11/15 | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | CDE ↗ |
Changes in the last 90 days
0 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.
- No matching records were found in the currently loaded source data; coverage dates are listed below.
Under review
0 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.
| Drug | Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|---|
| No matching records were found in the currently loaded source data; coverage dates are listed below. | |||||
Catalogue holder records
7 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.
| Drug | Marketing authorization holder | Manufacturer | Approval number | Approved | Catalogue category (source text) | View source |
|---|---|---|---|---|---|---|
| Oxcarbazepine Tablets | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20265711 | 2026/08/25 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| Oxcarbazepine Tablets | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20255934 | 2025/11/12 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| Vortioxetine Hydrobromide Tablets | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20254349 | 2025/05/27 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| Sodium Valproate Sustained-release Tablets(I) | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20249693 | 2024/12/06 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| Fluvoxamine Maleate Tablets | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20249611 | 2024/12/01 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| 布南色林片 · No verified English name | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H20243686 | 2024/05/15 | Generic approved under the new chemical-drug registration classification | CDE ↗ |
| Sodium Valproate Tablets | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | Hunan Sheng Xiang Zhong Pharmaceutical Co., Ltd. romanized | 国药准字H43020874 | 2021/07/22 | Drug that passed quality-and-efficacy consistency evaluation | CDE ↗ |
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.
| Name | Company / applicant | Registration number | Status | Source update date | View 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.
| Drug | Acceptance number | Application type | Accepted | Company / applicant | View 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.