Monthly
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Billed every month
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 2 applications
Current coverage may be incomplete
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.
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.
Loaded records: 10 distinct approval numbers and 9 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| 广州白云山医药集团股份有限公司白云山何济公制药厂 | 国药准字H10980249 | 8ml:80mg | Category B (乙) | XD01ACL079S004010100373 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004010101024 | NHSA |
| 江苏知原药业股份有限公司 | 国药准字H20066175 | 25ml:250mg | Category B (乙) | XD01ACL079S004010101486 | NHSA |
| 江西普丽尔药业有限公司 | 国药准字H20083313 | 1% | Category B (乙) | XD01ACL079S004010104370 | NHSA |
| 广州白云山医药集团股份有限公司白云山何济公制药厂 | 国药准字H10980249 | 8ml:80mg | Category B (乙) | XD01ACL079S004020100373 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004020101024 | NHSA |
| 江苏知原药业股份有限公司 | 国药准字H20066175 | 25ml:250mg | Category B (乙) | XD01ACL079S004020101486 | NHSA |
| 黑龙江天辰药业有限公司 | 国药准字H20033681 | 10ml:100mg | Category B (乙) | XD01ACL079S004020103790 | NHSA |
| 江西普丽尔药业有限公司 | 国药准字H20083313 | 1% | Category B (乙) | XD01ACL079S004020204370 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004030101024 | NHSA |
| 江苏知原药业股份有限公司 | 国药准字H20066175 | 25ml:250mg | Category B (乙) | XD01ACL079S004030101486 | NHSA |
| 江西普丽尔药业有限公司 | 国药准字H20083313 | 1% | Category B (乙) | XD01ACL079S004030104370 | NHSA |
| 黑龙江天辰药业有限公司 | 国药准字H20033681 | 10ml:100mg | Category B (乙) | XD01ACL079S004030203790 | NHSA |
| 黑龙江天辰药业有限公司 | 国药准字H20033681 | 10ml:100mg | Category B (乙) | XD01ACL079S004030303790 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004040101024 | NHSA |
| 江苏知原药业股份有限公司 | 国药准字H20066175 | 25ml:250mg | Category B (乙) | XD01ACL079S004040101486 | NHSA |
| 黑龙江天辰药业有限公司 | 国药准字H20033681 | 10ml:100mg | Category B (乙) | XD01ACL079S004040103790 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004050101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004060101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004070101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004080101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004090101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004100101024 | NHSA |
| 重庆青阳药业有限公司 | 国药准字H10950136 | 1% | Category B (乙) | XD01ACL079S004110101024 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001010101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001020101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001030101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001030201841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001040101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001050101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001060101841 | NHSA |
| 湖北潜龙药业有限公司 | 国药准字H20083747 | 每毫升含联苯苄唑0.01克 | Category B (乙) | XD01ACL079T001070101841 | NHSA |
| 北京华素制药股份有限公司 | 国药准字H10930042 | 1% | Not stated by source | XD01ACL079T002010100052 | NHSA |
| 福元药业有限公司 | 国药准字H20254937 | 1%(10 毫升:0.1克) | Not stated by source | XD01ACL079T002010180651 | NHSA |
| 深圳格莱恩生物医药科技有限公司 | 国药准字H20265676 | 1%(15ml:0.15g) | Not stated by source | XD01ACL079T002010185074 | NHSA |
| 福元药业有限公司 | 国药准字H20254937 | 1%(10 毫升:0.1克) | Not stated by source | XD01ACL079T002010280651 | NHSA |
| 北京华素制药股份有限公司 | 国药准字H10930042 | 1% | Not stated by source | XD01ACL079T002020100052 | NHSA |
| 福元药业有限公司 | 国药准字H20269163 | 1%(30ml:0.3g) | Not stated by source | XD01ACL079T002020180651 | 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: 15 filings and 14 distinct first applicants.
Generic 15
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 江苏和晨药业有限公司;江苏知原药业股份有限公司 | CYHS2502567 | Generic | 2025/07/17 | Not stated by source | CDE |
| 苏州高迈药业有限公司;唐山红星药业有限责任公司 | CYHS2601784 | Generic | 2026/07/27 | Not stated by source | CDE |
| 南京艾德凯腾生物医药有限责任公司;药大制药有限公司 | CYHS2501550 | Generic | 2025/04/24 | Not stated by source | CDE |
| 安徽省先锋制药有限公司 | CYHS2602117 | Generic | 2026/08/25 | Not stated by source | CDE |
| 安徽省先锋制药有限公司 | CYHS2602116 | Generic | 2026/08/25 | Not stated by source | CDE |
| 北京诚济制药股份有限公司 | CYHS2600356 | Generic | 2026/02/04 | Not stated by source | CDE |
| 国铭制药(海南)有限公司;杭州万邦天诚药业有限公司 | CYHS2503921 | Generic | 2025/11/11 | Not stated by source | CDE |
| 浙江百代医药科技有限公司;浙江赛默制药有限公司 | CYHS2503029 | Generic | 2025/08/19 | Not stated by source | CDE |
| 中山万汉制药有限公司 | CYHS2503009 | Generic | 2025/08/16 | Not stated by source | CDE |
| 杭州上禾健康科技有限公司;杭州万邦天诚药业有限公司 | CYHS2503005 | Generic | 2025/08/16 | Not stated by source | CDE |
| 安徽肽渡生物医药科技有限公司;浙江浙北药业有限公司 | CYHS2502740 | Generic | 2025/07/30 | Not stated by source | CDE |
| 浙江致新医药科技有限公司;浙江浙北药业有限公司 | CYHS2501987 | Generic | 2025/06/05 | Not stated by source | CDE |
| 重庆万霖生物医药科技有限公司;浙江赛默制药有限公司 | CYHS2501742 | Generic | 2025/05/14 | Not stated by source | CDE |
| 唐山红星药业有限责任公司 | CYHS2500881 | Generic | 2025/02/28 | Not stated by source | CDE |
| 安徽四环科宝制药有限公司 | CYHS2500716 | Generic | 2025/02/13 | Not stated by source | CDE |
Loaded records: 4 filings and 3 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 苏州高迈药业有限公司;唐山红星药业有限责任公司 | CYHS2601784 | Generic | 2026/07/27 | Not stated by source | CDE |
| 安徽省先锋制药有限公司 | CYHS2602117 | Generic | 2026/08/25 | Not stated by source | CDE |
| 安徽省先锋制药有限公司 | CYHS2602116 | Generic | 2026/08/25 | Not stated by source | CDE |
| 北京诚济制药股份有限公司 | CYHS2600356 | Generic | 2026/02/04 | Not stated by source | CDE |
Non-component matches: 7 companies with A status and 5 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 |
|---|---|---|---|---|---|---|
| 联苯苄唑 | 山东科新药业有限公司 | Y20260000797 | I | Exact ingredient | 2026/09/17 | CDE |
| 联苯苄唑 | 安徽皓元药业有限公司 | Y20260000497 | I | Exact ingredient | 2026/07/03 | CDE |
| 联苯苄唑 | 内蒙古京东药业有限公司 | Y20260000466 | I | Exact ingredient | 2026/07/01 | CDE |
| 联苯苄唑 | 安徽皓元药业有限公司 | Y20260000234 | I | Exact ingredient | 2026/04/29 | CDE |
| 联苯苄唑 | 湖北潜龙药业有限公司 | Y20260000228 | I | Exact ingredient | 2026/04/20 | CDE |
| 联苯苄唑 | 山东艾格林制药有限公司 | Y20250000590 | A | Exact ingredient | 2026/11/04 | CDE |
| 联苯苄唑 | 江苏诺泰澳赛诺生物制药股份有限公司 | Y20240000565 | A | Exact ingredient | 2026/06/02 | CDE |
| 联苯苄唑 | 中山万汉制药有限公司 | Y20230000786 | A | Exact ingredient | 2025/12/05 | CDE |
| 联苯苄唑 | Bayer Consumer Care AG | Y20190009219 | A | Exact ingredient | 2026/09/16 | CDE |
| 联苯苄唑 | 广州白云山汉方现代药业股份有限公司 | Y20190007629 | A | Exact ingredient | 2026/06/11 | CDE |
| 联苯苄唑 | 重庆青阳药业有限公司 | Y20190005392 | A | Exact ingredient | 2025/09/25 | CDE |
| 联苯苄唑 | 北京华素制药股份有限公司 | Y20170001211 | A | Exact ingredient | 2024/04/08 | 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: 2026/11/10 07:23. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.
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: 2026-10-26 to 2026-11-10; 0 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: 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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