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Emedastine Difumarate Eye Drops(富马酸依美斯汀滴眼液)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 2 applicationsNo longer listed under review: 1 application
Current coverage may be incomplete
Which companies are listed, and at what stages?
Each source is counted separately. Expand a list to inspect companies, identifiers, dates and sources.
Company names, approval identifiers and strengths are retained as recorded in the Chinese sources. Category labels include the original wording for verification.
Catalogue holders0View records ↓
Under-review filings8View records ↓
This year’s generic filers7View records ↓
NHSA approval numbers9View records ↓
API companies with A status6View records ↓
Chemical-drug catalogue
Loaded records: 0 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 |
|---|---|---|---|---|---|---|
| No matching records were found in the currently loaded source data; coverage dates are listed below. | ||||||
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.
NHSA drug codes
Loaded records: 9 distinct approval numbers and 8 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| 广州大光制药有限公司 | 国药准字H20264363 | 0.05%(5ml:2.5mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010100548 | NHSA |
| 成都普什制药有限公司 | 国药准字H20265504 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010102298 | NHSA |
| 石家庄四药有限公司 | 国药准字H20264359 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010102763 | NHSA |
| 山东博士伦福瑞达制药有限公司 | 国药准字H20065638 | 5ml:2.5mg(按依美斯汀计) | Category B (乙) | XS01GXY072G010010104072 | NHSA |
| 浙江视方极医药科技有限公司 | 国药准字H20255203 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010104693 | NHSA |
| Future Health Pharma GmbH | 国药准字HJ20181192 | 5ml:2.5mg(0.05%,以依美斯汀计) | Category B (乙) | XS01GXY072G010010178672 | NHSA |
| 苏州欧康维视生物科技有限公司 | 国药准字H20258020 | 0.05%(5ml:2.5mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010183562 | NHSA |
| 广州仁恒医药科技股份有限公司 | 国药准字H20254975 | 0.05%(5ml:2.5mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010184019 | NHSA |
| 成都普什制药有限公司 | 国药准字H20265504 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010202298 | NHSA |
| 石家庄四药有限公司 | 国药准字H20264359 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010202763 | NHSA |
| 浙江视方极医药科技有限公司 | 国药准字H20255203 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010204693 | NHSA |
| 成都普什制药有限公司 | 国药准字H20265504 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010302298 | NHSA |
| 浙江视方极医药科技有限公司 | 国药准字H20255203 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010304693 | NHSA |
| 浙江视方极医药科技有限公司 | 国药准字H20255203 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010010404693 | NHSA |
| 苏州欧康维视生物科技有限公司 | 国药准字H20269166 | 0.05%(0.35ml:0.175mg,按C₁₇H₂₆N₄O计) | Category B (乙) | XS01GXY072G010020183562 | 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.
Current under-review applications
Loaded records: 8 filings and 8 distinct first applicants.
Generic 8
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 江苏远恒药业有限公司 | CYHS2600924 | Generic | 2026/04/22 | Not stated by source | CDE |
| 四川健林药业有限责任公司;广州华圣制药有限公司 | CYHS2601751 | Generic | 2026/07/21 | Not stated by source | CDE |
| 北京普祺医药科技股份有限公司;湖北远大天天明制药有限公司 | CYHS2601726 | Generic | 2026/07/20 | Not stated by source | CDE |
| 珠海前列药业有限公司;湖南华纳大药厂股份有限公司 | CYHS2600832 | Generic | 2026/04/11 | Not stated by source | CDE |
| 北京汇恩兰德制药股份有限公司 | CYHS2600580 | Generic | 2026/02/28 | Not stated by source | CDE |
| 武汉益博元医药科技有限公司;北京汇恩兰德制药股份有限公司 | CYHS2504201 | Generic | 2025/12/06 | Not stated by source | CDE |
| 浙江赛默制药有限公司 | CYHS2602667 | Generic | 2026/10/30 | Not stated by source | CDE |
| 南京海纳医药科技股份有限公司;南京海纳制药有限公司 | CYHS2602671 | Generic | 2026/11/02 | Not stated by source | CDE |
New generic filings in 2026
Loaded records: 7 filings and 7 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 江苏远恒药业有限公司 | CYHS2600924 | Generic | 2026/04/22 | Not stated by source | CDE |
| 四川健林药业有限责任公司;广州华圣制药有限公司 | CYHS2601751 | Generic | 2026/07/21 | Not stated by source | CDE |
| 北京普祺医药科技股份有限公司;湖北远大天天明制药有限公司 | CYHS2601726 | Generic | 2026/07/20 | Not stated by source | CDE |
| 珠海前列药业有限公司;湖南华纳大药厂股份有限公司 | CYHS2600832 | Generic | 2026/04/11 | Not stated by source | CDE |
| 北京汇恩兰德制药股份有限公司 | CYHS2600580 | Generic | 2026/02/28 | Not stated by source | CDE |
| 浙江赛默制药有限公司 | CYHS2602667 | Generic | 2026/10/30 | Not stated by source | CDE |
| 南京海纳医药科技股份有限公司;南京海纳制药有限公司 | CYHS2602671 | Generic | 2026/11/02 | Not stated by source | CDE |
API registrations
Non-component matches: 6 companies with A status and 4 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 |
|---|---|---|---|---|---|---|
| 富马酸依美斯汀 | 江西科睿药业有限公司 | Y20260000177 | I | Exact ingredient | 2026/04/20 | CDE |
| 富马酸依美斯汀 | 山东绅联药业股份有限公司 | Y20260000072 | I | Exact ingredient | 2026/03/06 | CDE |
| 富马酸依美斯汀 | 赤峰赛林泰药业有限公司 | Y20250000964 | I | Exact ingredient | 2025/09/26 | CDE |
| 富马酸依美斯汀 | 宿州亿帆药业有限公司 | Y20250000809 | I | Exact ingredient | 2025/08/11 | CDE |
| 富马酸依美斯汀 | 甘肃皓天医药科技有限责任公司 | Y20240000093 | A | Exact ingredient | 2026/10/29 | CDE |
| 富马酸依美斯汀 | 吉林汇康制药有限公司 | Y20220001078 | A | Exact ingredient | 2025/03/13 | CDE |
| 富马酸依美斯汀 | 湖南九典宏阳制药有限公司 | Y20220000635 | A | Exact ingredient | 2025/07/08 | CDE |
| 富马酸依美斯汀 | SHIRATORI Pharmaceutical Co., Ltd. | Y20210001142 | A | Exact ingredient | 2025/08/31 | CDE |
| 富马酸依美斯汀 | 山东博士伦福瑞达制药有限公司 | Y20190001397 | A | Exact ingredient | 2024/09/04 | CDE |
| 富马酸依美斯汀 | 四川德峰药业有限公司 | Y20190001284 | A | Exact ingredient | 2023/03/24 | CDE |
| 富马酸依美斯汀 | 四川德峰药业有限公司 | Y20180001755 | A | Exact ingredient | 2023/10/31 | 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.
What changed recently?
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: 2026/11/10 07:23. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.
-
2026/11/02Accepted
南京海纳医药科技股份有限公司;南京海纳制药有限公司
CYHS2602671
Fact date: 2026/11/02 · Site observation date: 2026/11/03
View source ↗ -
2026/10/30Accepted
-
2026/10/28No longer listed under review
润尔眼科药物（广州）有限公司
CYHS2504223
Fact date: 2026/10/28 · Site observation date: 2026/10/28
Accepted: 2025/12/09
not on the CDE under-review list in this snapshot; the review / approval outcome is to be checked
View source ↗
How current is each source?
- CDE acceptances and review
- Last successful update: 2026/11/10 07:27
- Chemical-drug catalogue
- Last successful update: 2026/11/10 07:23
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.
- Full API register
- Last successful update: 2026/11/10 07:25
- NHSA drug codes
- Last successful update: 2026/11/05 06:45
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.
- NMPA drug delivery notices
- Last successful update: 2026/11/10 18:31
First index-page publication dates: 2026-10-26 to 2026-11-10; 0 pages pending. Covers loaded notices only, not a complete historical approval database.
- Drug Clinical Trial Registry and Information Disclosure Platform
- Last successful update: 2026/11/10 08:10 · Current coverage may be incomplete
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: 3/30; discovered pending details: 20. 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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