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Sign in to subscribeAs of 13 November 2026, for Bromfenac Sodium Eye Drops, 7 applications are listed as under review at China's CDE; 4 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 1 holder.
Companies, stages and changes, with each record available on this page.
Listed in the US FDA Orange Book as PROLENSA (NDA 203168, BAUSCH AND LOMB INC).
Last 90 days: Accepted: 3 applicationsNo longer listed under review: 1 applicationSupplement delivery: 1 application
Current coverage may be incomplete
The brand names come from the US FDA Orange Book and describe US listing records for this active ingredient. They do not indicate that products under these brand names are approved or sold in China, or that Chinese applicants are affiliated with US holders.
Orange Book source export date: 2026/11/06. Version: 2026-11-06.
Showing 4 of 4 distinct brand names.
A brand with different source forms or statuses can appear on multiple rows and in both groups. Distinct brand names are counted once globally, with a limit of five.
Verified official English dosage form: Eye Drops. Listings are grouped by the source dosage form and route; records without a clear correspondence are listed in the other group. Grouping does not establish product equivalence.
| Brand name | Applicant (source text) | Application number | Dosage form (source text) | Route (source text) | Marketing status (source text) | Approval date |
|---|---|---|---|---|---|---|
| PROLENSA | BAUSCH AND LOMB INC | NDA 203168 · Product no. 001 | SOLUTION/DROPS | OPHTHALMIC | HUMAN PRESCRIPTION DRUG | 2013/04/05 |
| BROMSITE | SUN PHARMACEUTICAL INDUSTRIES LTD | NDA 206911 · Product no. 001 | SOLUTION/DROPS | OPHTHALMIC | HUMAN PRESCRIPTION DRUG | 2016/04/08 |
| XIBROM | BAUSCH AND LOMB INC | NDA 021664 · Product no. 001 | SOLUTION/DROPS | OPHTHALMIC | DISCONTINUED | 2005/03/24 |
| BROMDAY | BAUSCH AND LOMB INC | NDA 021664 · Product no. 002 | SOLUTION/DROPS | OPHTHALMIC | DISCONTINUED | 2010/10/16 |
No listings in this group among the displayed brand names.
Same-form/route listings come first, followed by other forms/routes. Within each group, source prescription/OTC listings precede discontinued listings; unknown statuses are last. Each status bucket is ordered by earliest approval date, ascending: pre-1982 records first, missing dates last; ties by brand name, application number and product number. The first five distinct brands in this order are selected globally. All retained source facts for those brands are shown in their own groups; a brand spanning both groups counts once.
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: 1 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 0 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 |
|---|---|---|---|---|---|---|
| SENJU PHARMACEUTICAL CO., LTD. | SENJU PHARMACEUTICAL CO., LTD. Karatsu Plant | H20150243 | 2009/09/29 | See source | Imported originator drug | 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: 29 distinct approval numbers and 22 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Guangdong Zhong Sheng Pharma Co., Ltd. romanized | 国药准字H20233262 | See source | Category B | XS01BCX230G010010100371 | NHSA |
| Jin Yao He Ping (Tianjin) Pharmaceutical Co., Ltd. romanized | 国药准字H20213053 | See source | Category B | XS01BCX230G010010100952 | NHSA |
| Shenyang Xing Qi Yan Yao Co., Ltd. romanized | 国药准字H20244468 | See source | Category B | XS01BCX230G010010101322 | NHSA |
| Jiangsu Vanguard Pharmaceutical Co., Ltd. | 国药准字H20234193 | See source | Category B | XS01BCX230G010010101503 | NHSA |
| Wuhan Wu Jing Pharma Co., Ltd. romanized | 国药准字H20244284 | See source | Category B | XS01BCX230G010010101978 | NHSA |
| Chengdu Pusch Pharmaceutical Co., Ltd. | 国药准字H20256506 | See source | Category B | XS01BCX230G010010102298 | NHSA |
| Qilu Pharmaceutical Co., Ltd. | 国药准字H20183490 | See source | Category B | XS01BCX230G010010104021 | NHSA |
| Jinan Chen Xin Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20150022 | 5ml:5mg(0.1%) | Category B | XS01BCX230G010010104127 | NHSA |
| Hefei Hua Wei Pharma Co., Ltd. romanized | 国药准字H20244569 | See source | Category B | XS01BCX230G010010104388 | NHSA |
| Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | 国药准字H20253221 | See source | Category B | XS01BCX230G010010104693 | NHSA |
| Jiangxi Ma Ying Long Mei Kang Pharma Co., Ltd. romanized | 国药准字H20264422 | See source | Category B | XS01BCX230G010010105293 | NHSA |
| Qi Lu Pharmaceutical (Hainan) Co., Ltd. romanized | 国药准字H20233640 | See source | Category B | XS01BCX230G010010105847 | NHSA |
| Liaoning Mei Zi Lin Pharma Co., Ltd. romanized | 国药准字H20193244 | See source | Category B | XS01BCX230G010010106441 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010010109920 | NHSA |
| Hebei Chuang Jian Pharma Co., Ltd. romanized | 国药准字H20243677 | See source | Category B | XS01BCX230G010010110364 | NHSA |
| SENJU PHARMACEUTICAL CO.,LTD. | 国药准字HJ20150243 | See source | Category B | XS01BCX230G010010179077 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20213554 | See source | Category B | XS01BCX230G010010181567 | NHSA |
| Suzhou Ou Kang Wei Shi Bio Technology Co., Ltd. romanized | 国药准字H20253042 | See source | Category B | XS01BCX230G010010183562 | NHSA |
| Guangzhou Ren Heng Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20255727 | See source | Category B | XS01BCX230G010010184019 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20247205 | See source | Category B | XS01BCX230G010010184190 | NHSA |
| Chengdu Pusch Pharmaceutical Co., Ltd. | 国药准字H20256506 | See source | Category B | XS01BCX230G010010202298 | NHSA |
| Qilu Pharmaceutical Co., Ltd. | 国药准字H20183490 | See source | Category B | XS01BCX230G010010204021 | NHSA |
| Jinan Chen Xin Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20150022 | 5ml:5mg(0.1%) | Category B | XS01BCX230G010010204127 | NHSA |
| Guangzhou Ren Heng Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20255727 | See source | Category B | XS01BCX230G010010284019 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20247205 | See source | Category B | XS01BCX230G010010284190 | NHSA |
| Run Er Yan Ke Drug (Guangzhou) Co., Ltd. romanized | 国药准字H20244161 | See source | Category B | XS01BCX230G010010284784 | NHSA |
| Chengdu Pusch Pharmaceutical Co., Ltd. | 国药准字H20256506 | See source | Category B | XS01BCX230G010010302298 | NHSA |
| Jinan Chen Xin Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20150022 | 5ml:5mg(0.1%) | Category B | XS01BCX230G010010304127 | NHSA |
| Guangzhou Ren Heng Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20255727 | See source | Category B | XS01BCX230G010010384019 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20247205 | See source | Category B | XS01BCX230G010010384190 | NHSA |
| Chengdu Pusch Pharmaceutical Co., Ltd. | 国药准字H20256506 | See source | Category B | XS01BCX230G010010402298 | NHSA |
| Jinan Chen Xin Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20150022 | 5ml:5mg(0.1%) | Category B | XS01BCX230G010010404127 | NHSA |
| Guangzhou Ren Heng Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20255727 | See source | Category B | XS01BCX230G010010484019 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20247205 | See source | Category B | XS01BCX230G010010484190 | NHSA |
| Guangzhou Ren Heng Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20255727 | See source | Category B | XS01BCX230G010010584019 | NHSA |
| Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20247205 | See source | Category B | XS01BCX230G010010584190 | NHSA |
| Jin Yao He Ping (Tianjin) Pharmaceutical Co., Ltd. romanized | 国药准字H20223699 | See source | Category B | XS01BCX230G010020100952 | NHSA |
| Qilu Pharmaceutical Co., Ltd. | 国药准字H20183491 | See source | Category B | XS01BCX230G010020104021 | NHSA |
| Shandong Chen Xin Fu Dou Pharma Co., Ltd. romanized | 国药准字H20233366 | See source | Category B | XS01BCX230G010020104127 | NHSA |
| Zhejiang Sha Pu Ai Si Pharma Co., Ltd. romanized | 国药准字H20253220 | See source | Category B | XS01BCX230G010020104693 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243922 | See source | Category B | XS01BCX230G010020109920 | NHSA |
| Suzhou Ou Kang Wei Shi Bio Technology Co., Ltd. romanized | 国药准字H20263589 | See source | Category B | XS01BCX230G010020183562 | NHSA |
| Shandong Chen Xin Fu Dou Pharma Co., Ltd. romanized | 国药准字H20233366 | See source | Category B | XS01BCX230G010020204127 | NHSA |
| Shandong Chen Xin Fu Dou Pharma Co., Ltd. romanized | 国药准字H20233366 | See source | Category B | XS01BCX230G010020304127 | NHSA |
| Shandong Chen Xin Fu Dou Pharma Co., Ltd. romanized | 国药准字H20233366 | See source | Category B | XS01BCX230G010020404127 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010030109920 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010030209920 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010030309920 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010030409920 | NHSA |
| Zhongshan Wanhan Pharmaceuticals Co., Ltd. | 国药准字H20243868 | See source | Category B | XS01BCX230G010030509920 | NHSA |
| Ai Shi Pharmaceutical Co., Ltd. romanized | 国药准字H20264661 | See source | Category B | XS01BCX230G010010185580 | NHSA |
| Ai Shi Pharmaceutical Co., Ltd. romanized | 国药准字H20264662 | See source | Category B | XS01BCX230G010020185580 | 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: 7 filings and 6 distinct first applicants.
Generic 7
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Jiangsu Yuan Heng Pharma Co., Ltd. romanized | CYHS2602322 | Generic | 2026/09/17 | Not stated by source | CDE |
| Shandong Hai Shan Pharma Co., Ltd. romanized; Shandong Wei Zhi Bai Ke Pharma Co., Ltd. romanized | CYHS2602111 | Generic | 2026/08/25 | Not stated by source | CDE |
| Shijiazhuang No.4 Pharmaceutical Co., Ltd. | CYHS2601517 | Generic | 2026/06/26 | Not stated by source | CDE |
| Guangdong Nan Guo Pharma Co., Ltd. romanized | CYHS2601081 | Generic | 2026/05/12 | Not stated by source | CDE |
| Shijiazhuang Gree Pharmaceutical Co., Ltd | CYHS2504444 | Generic | 2025/12/27 | Not stated by source | CDE |
| Shijiazhuang Gree Pharmaceutical Co., Ltd | CYHS2504443 | Generic | 2025/12/27 | Not stated by source | CDE |
| Hubei Mei Lin Pharma Co., Ltd. romanized | CYHS2503161 | Generic | 2025/08/29 | Not stated by source | CDE |
Loaded records: 4 filings and 4 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Jiangsu Yuan Heng Pharma Co., Ltd. romanized | CYHS2602322 | Generic | 2026/09/17 | Not stated by source | CDE |
| Shandong Hai Shan Pharma Co., Ltd. romanized; Shandong Wei Zhi Bai Ke Pharma Co., Ltd. romanized | CYHS2602111 | Generic | 2026/08/25 | Not stated by source | CDE |
| Shijiazhuang No.4 Pharmaceutical Co., Ltd. | CYHS2601517 | Generic | 2026/06/26 | Not stated by source | CDE |
| Guangdong Nan Guo Pharma Co., Ltd. romanized | CYHS2601081 | Generic | 2026/05/12 | Not stated by source | CDE |
Non-component matches: 14 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 |
|---|---|---|---|---|---|---|
| 溴芬酸钠 · No verified English name | Shijiazhuang Gree Pharmaceutical Co., Ltd | Y20250000320 | A | Exact ingredient | 2026/10/12 | CDE |
| 溴芬酸钠 · No verified English name | Zhejiang Sai Mo Pharmaceutical Co., Ltd. romanized | Y20240000502 | A | Exact ingredient | 2025/12/17 | CDE |
| 溴芬酸钠 · No verified English name | Medilux Laboratories Pvt. Ltd | Y20230000372 | A | Exact ingredient | 2026/07/12 | CDE |
| 溴芬酸钠 · No verified English name | Zhongshan Wanhan Pharmaceuticals Co., Ltd. | Y20220000433 | A | Exact ingredient | 2024/03/11 | CDE |
| 溴芬酸钠 · No verified English name | Hebei An Jian Cheng Yi Pharmaceuticals Technology Co., Ltd. romanized | Y20210000778 | A | Exact ingredient | 2024/04/09 | CDE |
| 溴芬酸钠 · No verified English name | Guangzhou Hua Sheng Pharmaceutical Co., Ltd. romanized | Y20210000006 | A | Exact ingredient | 2025/04/16 | CDE |
| 溴芬酸钠 · No verified English name | Guangdong Xian Qiang Pharma Co., Ltd. romanized | Y20200001049 | A | Exact ingredient | 2025/03/27 | CDE |
| 溴芬酸钠 · No verified English name | YS Life Science Co., Ltd. | Y20190021249 | A | Exact ingredient | 2024/07/27 | CDE |
| 溴芬酸钠 · No verified English name | Wuhan Xian Lu Pharmaceuticals Technology Co., Ltd. romanized | Y20190000875 | A | Exact ingredient | 2026/06/02 | CDE |
| 溴芬酸钠 · No verified English name | Shandong Chen Long Pharma Co., Ltd. romanized | Y20190001971 | A | Exact ingredient | 2024/09/27 | CDE |
| 溴芬酸钠 · No verified English name | Jin Yao Pharma Co., Ltd. romanized | Y20170002121 | A | Exact ingredient | 2025/06/12 | CDE |
| 溴芬酸钠 · No verified English name | Indoco Remedies Ltd. (Kilo Lab) | Y20170001316 | A | Exact ingredient | 2026/05/06 | CDE |
| 溴芬酸钠 · No verified English name | Qilu Pharmaceutical Co., Ltd. | Y20170000569 | A | Exact ingredient | 2024/09/04 | CDE |
| 溴芬酸钠 · No verified English name | Liaoning Tian Long Pharma Co., Ltd. romanized | Y20170000249 | A | Exact ingredient | 2024/09/12 | 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.
CYHS2502163
Fact date: 2026/10/29 · Site observation date: 2026/10/29
Accepted: 2025/06/17
not on the CDE under-review list in this snapshot; the review / approval outcome is to be checked
View source ↗CYHB2601321 · 国药准字H20269252
Fact date: 2026/10/16 · Publication date: 2026/10/19 · Site observation date: 2026/11/03
Supplemental application; excluded from new marketing approvals.
View source · Table row 7 ↗CYHS2602322
Fact date: 2026/09/17 · Site observation date: 2026/10/21
View source ↗CYHS2602111
Fact date: 2026/08/25 · Site observation date: 2026/10/22
View source ↗JYHB2600490
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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