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Sign in to subscribeAs of 13 November 2026, for Ibuprofen Injection, 8 applications are listed as under review at China's CDE; 4 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 2 holders.
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 7 applications
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: 2 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 2 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 |
|---|---|---|---|---|---|---|
| Chengdu Shuo De Pharma Co., Ltd. romanized | Chengdu Easton Biopharmaceuticals Co.,Ltd. | 国药准字 H20234488 | 2023/11/14 | 2ml:10mg | Generic approved under the new chemical-drug registration classification | CDE |
| Name not romanized | Chengdu Easton Biopharmaceuticals Co.,Ltd. | 国药准字H20183345 | 2018/07/31 | 8ml:0.8g | Generic approved under the new chemical-drug registration classification | CDE |
| Name not romanized | Chengdu Easton Biopharmaceuticals Co.,Ltd. | 国药准字H20183344 | 2018/07/31 | 4ml:0.4g | 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: 7 distinct approval numbers and 4 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20203473 | 4ml:0.4g | Category B | XM01AEB173B002010102013 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203061 | 4ml:0.4g | Category B | XM01AEB173B002010103492 | NHSA |
| Chengdu Shuo De Pharma Co., Ltd. romanized | 国药准字H20234488 | 2ml:10mg | Category B | XM01AEB173B002010183830 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20203473 | 4ml:0.4g | Category B | XM01AEB173B002010202013 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203061 | 4ml:0.4g | Category B | XM01AEB173B002010203492 | NHSA |
| Shaanxi Li Cai Pharma Co., Ltd. romanized | 国药准字H20203317 | 4ml:0.4g | Category B | XM01AEB173B002010204494 | NHSA |
| Chengdu Shuo De Pharma Co., Ltd. romanized | 国药准字H20234488 | 2ml:10mg | Category B | XM01AEB173B002010283830 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203061 | 4ml:0.4g | Category B | XM01AEB173B002010303492 | NHSA |
| Shaanxi Li Cai Pharma Co., Ltd. romanized | 国药准字H20203317 | 4ml:0.4g | Category B | XM01AEB173B002010304494 | NHSA |
| Shaanxi Li Cai Pharma Co., Ltd. romanized | 国药准字H20203317 | 4ml:0.4g | Category B | XM01AEB173B002010404494 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20203474 | 8ml:0.8g | Category B | XM01AEB173B002020102013 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203060 | 8ml:0.8g | Category B | XM01AEB173B002020103492 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20203474 | 8ml:0.8g | Category B | XM01AEB173B002020202013 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203060 | 8ml:0.8g | Category B | XM01AEB173B002020203492 | NHSA |
| Shaanxi Li Cai Pharma Co., Ltd. romanized | 国药准字H20203318 | 8ml:0.8g | Category B | XM01AEB173B002020204494 | NHSA |
| Jilin Si Huan Pharmaceutical Co., Ltd. romanized | 国药准字H20203060 | 8ml:0.8g | Category B | XM01AEB173B002020303492 | NHSA |
| Shaanxi Li Cai Pharma Co., Ltd. romanized | 国药准字H20203318 | 8ml:0.8g | Category B | XM01AEB173B002020304494 | 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: 8 filings and 4 distinct first applicants.
Generic 8
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Zhong Fu Pharma Co., Ltd. romanized | CYHS2602108 | Generic | 2026/08/24 | Not stated by source | CDE |
| Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Zhong Fu Pharma Co., Ltd. romanized | CYHS2602107 | Generic | 2026/08/24 | Not stated by source | CDE |
| SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | CYHS2601110 | Generic | 2026/05/13 | Not stated by source | CDE |
| SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | CYHS2601109 | Generic | 2026/05/13 | Not stated by source | CDE |
| Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized | CYHS2602751 | Generic | 2026/11/09 | Not stated by source | CDE |
| Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized | CYHS2602750 | Generic | 2026/11/09 | Not stated by source | CDE |
| Zhengzhou Zhuo Feng Pharmaceutical Co., Ltd. romanized | CYHS2602772 | Generic | 2026/11/11 | Not stated by source | CDE |
| Zhengzhou Zhuo Feng Pharmaceutical Co., Ltd. romanized | CYHS2602771 | Generic | 2026/11/11 | Not stated by source | CDE |
Loaded records: 8 filings and 4 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Zhong Fu Pharma Co., Ltd. romanized | CYHS2602108 | Generic | 2026/08/24 | Not stated by source | CDE |
| Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Zhong Fu Pharma Co., Ltd. romanized | CYHS2602107 | Generic | 2026/08/24 | Not stated by source | CDE |
| SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | CYHS2601110 | Generic | 2026/05/13 | Not stated by source | CDE |
| SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | CYHS2601109 | Generic | 2026/05/13 | Not stated by source | CDE |
| Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized | CYHS2602751 | Generic | 2026/11/09 | Not stated by source | CDE |
| Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized | CYHS2602750 | Generic | 2026/11/09 | Not stated by source | CDE |
| Zhengzhou Zhuo Feng Pharmaceutical Co., Ltd. romanized | CYHS2602772 | Generic | 2026/11/11 | Not stated by source | CDE |
| Zhengzhou Zhuo Feng Pharmaceutical Co., Ltd. romanized | CYHS2602771 | Generic | 2026/11/11 | Not stated by source | CDE |
Non-component matches: 11 companies with A status and 2 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 |
|---|---|---|---|---|---|---|
| 布洛芬 · No verified English name | Yun Peng Pharmaceuticals Group Co., Ltd. romanized | Y20260000554 | I | Exact ingredient | 2026/07/23 | CDE |
| 布洛芬 · No verified English name | SMS Pharmaceutical Limited | Y20230001192 | I | Exact ingredient | 2024/01/09 | CDE |
| 布洛芬 · No verified English name | Ren He Tang Pharma Co., Ltd. romanized | Y20210001112 | A | Exact ingredient | 2025/06/03 | CDE |
| 布洛芬 · No verified English name | IOL Chemicals and Pharmaceuticals Ltd. | Y20220000857 | A | Exact ingredient | 2025/02/26 | CDE |
| 布洛芬 · No verified English name | SOLARA ACTIVE PHARMA SCIENCES LIMITED | Y20210000499 | A | Exact ingredient | 2023/03/24 | CDE |
| 布洛芬 · No verified English name | Zhuhai Run Dou Pharmaceutical Co., Ltd. romanized | Y20210000195 | A | Exact ingredient | 2026/06/18 | CDE |
| 布洛芬 · No verified English name | SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | Y20190009435 | A | Exact ingredient | — | CDE |
| 布洛芬 · No verified English name | Hubei Heng Di Pharma Co., Ltd. romanized | Y20190008553 | A | Exact ingredient | 2025/08/27 | CDE |
| 布洛芬 · No verified English name | Huadong Medicine (Xi’an)Bodyguard Pharmaceutical Co.,Ltd. | Y20190006681 | A | Exact ingredient | — | CDE |
| 布洛芬 · No verified English name | Hao Yi Sheng Pharma Group Co., Ltd. romanized | Y20190005969 | A | Exact ingredient | — | CDE |
| 布洛芬 · No verified English name | Tai Shan Shi Xin Ning Pharmaceutical Co., Ltd. romanized | Y20190003234 | A | Exact ingredient | 2026/02/28 | CDE |
| 布洛芬 · No verified English name | Hua Zhong Pharma Co., Ltd. romanized | Y20190003113 | A | Exact ingredient | 2025/06/11 | CDE |
| 布洛芬 · No verified English name | Zi Bo Xin Hua - Bai Li Gao Pharmaceutical Co., Ltd. romanized | Y20190002336 | A | Exact ingredient | 2024/07/27 | CDE |
| 布洛芬 · No verified English name | SHANDONG XINHUA PHARMACEUTICAL COMPANY LIMITED | Y20180001074 | A | Exact ingredient | 2024/09/04 | CDE |
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.
CYHS2602772
Fact date: 2026/11/11 · Site observation date: 2026/11/12
View source ↗CYHS2602771
Fact date: 2026/11/11 · Site observation date: 2026/11/12
View source ↗CYHS2602751
Fact date: 2026/11/09 · Site observation date: 2026/11/10
View source ↗CYHS2602750
Fact date: 2026/11/09 · Site observation date: 2026/11/10
View source ↗CYHB2601736
Fact date: 2026/09/15 · Site observation date: 2026/10/22
View source ↗CYHS2602108
Fact date: 2026/08/24 · Site observation date: 2026/10/22
View source ↗CYHS2602107
Fact date: 2026/08/24 · 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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