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Sign in to subscribeAs of 13 November 2026, for Sodium Acetate Ringer's Injection, 2 applications are listed as under review at China's CDE; 2 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 11 holders.
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 1 application
Current coverage may be incomplete
Each source is counted separately. Expand a list to inspect companies, identifiers, dates and sources.
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.
Loaded records: 11 holders; 6 in the quality-and-efficacy consistency-evaluation category, and 5 in the new chemical-registration-classification generic category. Category counts may overlap.
| Marketing authorization holder | Manufacturer | Approval number | Approved | Strength / specification | Catalogue category (source text) | View source |
|---|---|---|---|---|---|---|
| Xian Jing Xi Shuang He Pharma Co., Ltd. romanized | Xian Jing Xi Shuang He Pharma Co., Ltd. romanized | 国药准字H20263484 | 2026/02/25 | 500ml | Generic approved under the new chemical-drug registration classification | CDE |
| Zhejiang Kang Ji Er Pharma Co., Ltd. romanized | Zhejiang Kang Ji Er Pharma Co., Ltd. romanized | 国药准字H20254266 | 2025/05/27 | 500ml | Generic approved under the new chemical-drug registration classification | CDE |
| Hubei Duo Rui Pharma Co., Ltd. romanized | Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20205069 | 2024/10/21 | 250ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | 国药准字H20193277 | 2024/04/19 | 500ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | 国药准字H20183266 | 2024/04/01 | 500ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | 国药准字H20247060 | 2024/04/01 | 250ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Hubei Duo Rui Pharma Co., Ltd. romanized | Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20163331 | 2023/10/24 | 500ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Guizhou Ke Lun Pharma Co., Ltd. romanized | Guizhou Ke Lun Pharma Co., Ltd. romanized | 国药准字H20183036 | 2023/06/09 | See source | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Shijiazhuang No.4 Pharmaceutical Co., Ltd. | Shijiazhuang No.4 Pharmaceutical Co., Ltd. | 国药准字H20173310 | 2023/05/04 | 500ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Hunan Ke Lun Pharmaceutical Co., Ltd. romanized | Hunan Ke Lun Pharmaceutical Co., Ltd. romanized | 国药准字H20173311 | 2023/05/04 | 500ml | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Suzhou Lang Yi Biopharmaceuticals Research Co., Ltd. romanized | Hebei Tian Cheng Pharma Co., Ltd. romanized | 国药准字H20233216 | 2023/02/21 | 500ml | Generic approved under the new chemical-drug registration classification | CDE |
| Henan Ke Lun Pharma Co., Ltd. romanized | Henan Ke Lun Pharma Co., Ltd. romanized | 国药准字H20233013 | 2023/01/09 | 500ml | Generic approved under the new chemical-drug registration classification | CDE |
| Hebei Ren He Yi Kang Pharma Co., Ltd. romanized | Hebei Ren He Yi Kang Pharma Co., Ltd. romanized | 国药准字H20223877 | 2022/11/22 | See source | Generic approved under the new chemical-drug registration classification | CDE |
Distinct full holder names; manufacturers are used only where the holder is unstated. The catalogue covers only part of the chemical-drug market. Categories are counted as recorded, not as a complete market census.
Loaded records: 15 distinct approval numbers and 12 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Tian Sheng Pharmaceutical Group Co., Ltd. romanized | 国药准字H20234195 | 500ml | Not stated by source | XB05BBC143B002010101055 | NHSA |
| Xian Jing Xi Shuang He Pharma Co., Ltd. romanized | 国药准字H20263484 | 500ml | Not stated by source | XB05BBC143B002010102492 | NHSA |
| Shijiazhuang No.4 Pharmaceutical Co., Ltd. | 国药准字H20173310 | 500ml | Not stated by source | XB05BBC143B002010102763 | NHSA |
| Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | 国药准字H20183266 | 500ml | Not stated by source | XB05BBC143B002010102964 | NHSA |
| Fujian Pin Teng Pharma Co., Ltd. romanized | 国药准字H20233013 | 500ml | Not stated by source | XB05BBC143B002010103063 | NHSA |
| Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | 国药准字H20193277 | 500ml | Not stated by source | XB05BBC143B002010104693 | NHSA |
| Zhejiang Kang Ji Er Pharma Co., Ltd. romanized | 国药准字H20254266 | 500ml | Not stated by source | XB05BBC143B002010104745 | NHSA |
| Hunan Ke Lun Pharmaceutical Co., Ltd. romanized | 国药准字H20173311 | 500ml | Not stated by source | XB05BBC143B002010104948 | NHSA |
| Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20163331 | 500ml | Not stated by source | XB05BBC143B002010106652 | NHSA |
| Guizhou Ke Lun Pharma Co., Ltd. romanized | 国药准字H20183036 | 500ml | Not stated by source | XB05BBC143B002010110242 | NHSA |
| Hebei Ren He Yi Kang Pharma Co., Ltd. romanized | 国药准字H20223877 | 500ml | Not stated by source | XB05BBC143B002010110349 | NHSA |
| Suzhou Lang Yi Biopharmaceuticals Research Co., Ltd. romanized | 国药准字H20233216 | 500ml | Not stated by source | XB05BBC143B002010183610 | NHSA |
| Fujian Pin Teng Pharma Co., Ltd. romanized | 国药准字H20233013 | 500ml | Not stated by source | XB05BBC143B002010203063 | NHSA |
| Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20163331 | 500ml | Not stated by source | XB05BBC143B002010206652 | NHSA |
| Guizhou Ke Lun Pharma Co., Ltd. romanized | 国药准字H20183036 | 500ml | Not stated by source | XB05BBC143B002010210242 | NHSA |
| Shijiazhuang No.4 Pharmaceutical Co., Ltd. | 国药准字H20173310 | 500ml | Not stated by source | XB05BBC143B002020102763 | NHSA |
| Shi Yao Yin Hu Pharmaceutical Co., Ltd. romanized | 国药准字H20247060 | 250ml | Not stated by source | XB05BBC143B002020102964 | NHSA |
| Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | 国药准字H20247076 | 250ml | Not stated by source | XB05BBC143B002020104693 | NHSA |
| Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20205069 | 250ml | Not stated by source | XB05BBC143B002020106652 | NHSA |
| Hebei Ren He Yi Kang Pharma Co., Ltd. romanized | 国药准字H20223877 | 500ml | Not stated by source | XB05BBC143B002020110349 | NHSA |
| Hubei Duo Rui Pharma Co., Ltd. romanized | 国药准字H20205069 | 250ml | Not stated by source | XB05BBC143B002030106652 | NHSA |
Approval numbers and companies are deduplicated separately; packaging records remain individually listed. An empty insurance class means it is unstated. NHSA codes supply no approval date and do not establish the outcome of an acceptance number.
Loaded records: 2 filings and 2 distinct first applicants.
Generic 2
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Hubei Zhang Lian Du Lei Pharmaceutical Co., Ltd. romanized | CYHS2602525 | Generic | 2026/10/14 | Not stated by source | CDE |
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2600203 | Generic | 2026/01/16 | Not stated by source | CDE |
Loaded records: 2 filings and 2 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Hubei Zhang Lian Du Lei Pharmaceutical Co., Ltd. romanized | CYHS2602525 | Generic | 2026/10/14 | Not stated by source | CDE |
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2600203 | Generic | 2026/01/16 | Not stated by source | CDE |
Non-component matches: 0 companies with A status and 0 I-status records. Component matches are listed separately and excluded from these counts.
| Name | Company / applicant | Registration number | Status | Name match | Source update date | View source |
|---|---|---|---|---|---|---|
| No matching records were found in the currently loaded source data; coverage dates are listed below. | ||||||
A/I are source statuses. Matching uses exact ingredients, salt-normalized names and maintained combination components, without fuzzy matching. A-status companies are deduplicated by the first registered company. Components are excluded from headline counts; the register does not identify the associated formulation.
Last 90 days, ordered by fact date. Marketing approvals, trial registrations, supplements, notices and review changes are labelled separately.
Trial registration does not mean an application will follow.
This product is outside the trial-registration backfill scope. New registrations after daily collection started remain in scope. Historical rows may also be found by another product search; neither implies complete historical coverage for this product.
NHSA edition maintained to 2026-10-23; latest successful catalogue check: 2026/11/13 06:39. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.
This source was last successfully updated at 2026/11/12 18:32; current coverage may be incomplete.
CYHS2602525
Fact date: 2026/10/14 · Site observation date: 2026/10/22
View source ↗Distinct full holder names; manufacturers are used only where the holder is unstated. The catalogue covers only part of the chemical-drug market. Categories are counted as recorded, not as a complete market census.
The fully loaded edition was maintained to 2026-10-23. Publication lags maintenance: the verified 2026-10-16 edition was published on 10-28, a 12-day gap. This is not a fixed lag for every edition.
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.
Daily collection reads new registrations. Backfill covers registration numbers from 2025 onward (CTR2025/CTR2026), not first-publication years. States are dated observations; revisions are not tracked.
This product is outside the trial-registration backfill scope. New registrations after daily collection started remain in scope. Historical rows may also be found by another product search; neither implies complete historical coverage for this product.
Public-product searches scanned: 7/30; discovered pending details: 13. Record counts in unscanned portions remain unknown.
Filings are counted by acceptance number and filing companies by first applicant. Strengths may have separate applications. Drug names are normalized only for width and whitespace; distinct generic names, dosage forms and combinations remain separate. Unstated strengths are marked. Company counts from different sources must not be added together.
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.
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