Monthly
US$200
Billed every month
Metoprolol Succinate Extended-release Capsules(琥珀酸美托洛尔缓释胶囊)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 2 applications
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 holders6View records ↓
Under-review filings4View records ↓
This year’s generic filers2View records ↓
NHSA approval numbers10View records ↓
API companies with A status19View records ↓
Chemical-drug catalogue
Loaded records: 6 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 6 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 |
|---|---|---|---|---|---|---|
| 上海惠永制药有限公司 | 上海惠永制药有限公司 | 国药准字H20263856 | 2026/04/07 | 47.5mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 桂林华信制药有限公司 | 桂林华信制药有限公司 | 国药准字H20256269 | 2025/12/16 | 95mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 桂林华信制药有限公司 | 桂林华信制药有限公司 | 国药准字H20256270 | 2025/12/16 | 23.75mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 杭州沐源生物医药科技有限公司 | 宁波美诺华天康药业有限公司 | 国药准字H20256182 | 2025/12/09 | 47.5mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 福建省宝诺医药研发有限公司 | 浙江京新药业股份有限公司 | 国药准字H20249096 | 2024/10/16 | 47.5mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 烟台鲁银药业有限公司 | 烟台鲁银药业有限公司 | 国药准字H20244200 | 2024/06/28 | 47.5mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 烟台鲁银药业有限公司 | 烟台鲁银药业有限公司 | 国药准字H20244199 | 2024/06/28 | 95mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 烟台鲁银药业有限公司 | 烟台鲁银药业有限公司 | 国药准字H20244198 | 2024/06/28 | 23.75mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 辰欣药业股份有限公司 | 辰欣药业股份有限公司 | 国药准字H20243717 | 2024/05/15 | 以琥珀酸美托洛尔计：47.5mg（主要成份与酒石酸美托洛尔50mg相当） | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 辰欣药业股份有限公司 | 辰欣药业股份有限公司 | 国药准字H20243716 | 2024/05/15 | 以琥珀酸美托洛尔计：23.75mg（主要成份与酒石酸美托洛尔25mg相当） | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | 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.
NHSA drug codes
Loaded records: 10 distinct approval numbers and 6 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010104127 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244199 | 95mg | Category B (乙) | XC07ABM062E003010104240 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256270 | 23.75mg | Category B (乙) | XC07ABM062E003010105199 | NHSA |
| 福建省宝诺医药研发有限公司 | 国药准字H20249096 | 47.5mg | Category B (乙) | XC07ABM062E003010183544 | NHSA |
| 杭州沐源生物医药科技股份有限公司 | 国药准字H20256182 | 47.5mg | Category B (乙) | XC07ABM062E003010184135 | NHSA |
| 上海惠永制药有限公司 | 国药准字H20263856 | 47.5mg | Category B (乙) | XC07ABM062E003010185534 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010204127 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256270 | 23.75mg | Category B (乙) | XC07ABM062E003010205199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010304127 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256270 | 23.75mg | Category B (乙) | XC07ABM062E003010305199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010404127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010504127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010604127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010704127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010804127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003010904127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011004127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011104127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011204127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011304127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011404127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011504127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011604127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011704127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011804127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003011904127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243716 | 23.75mg | Category B (乙) | XC07ABM062E003012004127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020104127 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244198 | 23.75mg | Category B (乙) | XC07ABM062E003020104240 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256269 | 95mg | Category B (乙) | XC07ABM062E003020105199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020204127 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256269 | 95mg | Category B (乙) | XC07ABM062E003020205199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020304127 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256269 | 95mg | Category B (乙) | XC07ABM062E003020305199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020404127 | NHSA |
| 桂林华信制药有限公司 | 国药准字H20256269 | 95mg | Category B (乙) | XC07ABM062E003020405199 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020504127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020604127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020704127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020804127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003020904127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021004127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021104127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021204127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021304127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021404127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021504127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021604127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021704127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021804127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003021904127 | NHSA |
| 辰欣药业股份有限公司 | 国药准字H20243717 | 47.5mg | Category B (乙) | XC07ABM062E003022004127 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030104240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030204240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030304240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030404240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030504240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030604240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030704240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030804240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003030904240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003031004240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003031104240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003031204240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003040104240 | NHSA |
| 烟台鲁银药业有限公司 | 国药准字H20244200 | 47.5mg | Category B (乙) | XC07ABM062E003050104240 | 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: 4 filings and 2 distinct first applicants.
Generic 4
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 吉林天衡英睿制药有限公司 | CYHS2602343 | Generic | 2026/09/20 | Not stated by source | CDE |
| 吉林天衡英睿制药有限公司 | CYHS2602342 | Generic | 2026/09/20 | Not stated by source | CDE |
| 山东华素制药有限公司 | CYHS2601415 | Generic | 2026/06/15 | Not stated by source | CDE |
| 山东华素制药有限公司 | CYHS2601414 | Generic | 2026/06/15 | Not stated by source | CDE |
New generic filings in 2026
Loaded records: 4 filings and 2 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 吉林天衡英睿制药有限公司 | CYHS2602343 | Generic | 2026/09/20 | Not stated by source | CDE |
| 吉林天衡英睿制药有限公司 | CYHS2602342 | Generic | 2026/09/20 | Not stated by source | CDE |
| 山东华素制药有限公司 | CYHS2601415 | Generic | 2026/06/15 | Not stated by source | CDE |
| 山东华素制药有限公司 | CYHS2601414 | Generic | 2026/06/15 | Not stated by source | CDE |
API registrations
Non-component matches: 19 companies with A status and 7 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 |
|---|---|---|---|---|---|---|
| 酒石酸美托洛尔 | 安徽诺尔康药业有限公司 | Y20260000444 | I | Salt-normalized ingredient | 2026/07/16 | CDE |
| 琥珀酸美托洛尔 | 安徽诺尔康药业有限公司 | Y20260000462 | I | Exact ingredient | 2026/07/03 | CDE |
| 琥珀酸美托洛尔 | Sun Pharmaceutical Industries Limited | Y20240001575 | I | Exact ingredient | 2025/04/16 | CDE |
| 酒石酸美托洛尔 | Atul Bioscience Ltd | Y20240001015 | I | Salt-normalized ingredient | 2025/02/17 | CDE |
| 琥珀酸美托洛尔 | Ipca Laboratories Limited | Y20230001162 | A | Exact ingredient | 2026/04/03 | CDE |
| 酒石酸美托洛尔 | 白云山东泰商丘药业有限公司 | Y20240000368 | A | Salt-normalized ingredient | 2025/12/09 | CDE |
| 琥珀酸美托洛尔 | 山东华素制药有限公司 | Y20240000199 | A | Exact ingredient | 2026/09/21 | CDE |
| 琥珀酸美托洛尔 | ATUL BIOSCIENCE LTD. | Y20230000090 | A | Exact ingredient | 2024/11/26 | CDE |
| 琥珀酸美托洛尔 | 桂林华信制药有限公司 | Y20230000348 | A | Exact ingredient | 2026/03/12 | CDE |
| 酒石酸美托洛尔 | Ipca Laboratories Limited | Y20220000474 | A | Salt-normalized ingredient | 2024/08/07 | CDE |
| 琥珀酸美托洛尔 | Dr.Reddy's Laboratories Ltd. | Y20220000109 | A | Exact ingredient | 2024/01/16 | CDE |
| 琥珀酸美托洛尔 | 山东齐都药业有限公司 | Y20210000268 | A | Exact ingredient | 2026/08/25 | CDE |
| 琥珀酸美托洛尔 | CTX Lifesciences Pvt. Ltd. | Y20190021559 | A | Exact ingredient | 2026/09/17 | CDE |
| 琥珀酸美托洛尔 | 浙江华海药业股份有限公司 | Y20200001420 | A | Exact ingredient | 2023/07/06 | CDE |
| 琥珀酸美托洛尔 | 山东新时代药业有限公司 | Y20200000203 | A | Exact ingredient | 2026/04/27 | CDE |
| 酒石酸美托洛尔 | AstraZeneca AB | Y20190009941 | A | Salt-normalized ingredient | — | CDE |
| 酒石酸美托洛尔 | AstraZeneca AB | Y20190009940 | A | Salt-normalized ingredient | — | CDE |
| 酒石酸美托洛尔 | 浙江普洛家园药业有限公司 | Y20190009774 | A | Salt-normalized ingredient | 2025/11/25 | CDE |
| 酒石酸美托洛尔 | 广州白云山汉方现代药业股份有限公司 | Y20190007575 | A | Salt-normalized ingredient | 2026/06/17 | CDE |
| 酒石酸美托洛尔 | 上海信谊百路达药业有限公司 | Y20190006716 | A | Salt-normalized ingredient | 2023/03/24 | CDE |
| 酒石酸美托洛尔 | 常州四药制药有限公司 | Y20190004561 | A | Salt-normalized ingredient | 2026/03/18 | CDE |
| 琥珀酸美托洛尔 | 浙江普洛家园药业有限公司 | Y20190000080 | A | Exact ingredient | 2026/04/08 | CDE |
| 琥珀酸美托洛尔 | 浙江海翔川南药业有限公司 | Y20180001385 | A | Exact ingredient | 2026/10/28 | CDE |
| 酒石酸美托洛尔 | AstraZeneca AB | Y20170001948 | A | Salt-normalized ingredient | 2024/09/24 | CDE |
| 酒石酸美托洛尔 | AstraZeneca AB | Y20170001947 | A | Salt-normalized ingredient | 2024/09/24 | CDE |
| 酒石酸美托洛尔 | Sun Pharmaceutical Industries Limited | Y20170001466 | A | Salt-normalized ingredient | 2024/11/07 | CDE |
| 琥珀酸美托洛尔 | MOEHS IBERICA S.L. | Y20170001403 | A | Exact ingredient | 2026/10/16 | CDE |
| 琥珀酸美托洛尔 | 生泰合成工業股份有限公司 | Y20170001066 | I | Exact ingredient | — | CDE |
| 琥珀酸美托洛尔 | POLYDRUG LABORATORIES PVT. LTD. | Y20170001016 | I | Exact ingredient | — | CDE |
| 酒石酸美托洛尔 | POLYDRUG LABORATORIES PVT. LTD. | Y20170000942 | I | Salt-normalized ingredient | — | CDE |
| 酒石酸美托洛尔 | CTX Lifesciences Pvt. Ltd. | Y20170000853 | A | Salt-normalized ingredient | 2026/01/02 | CDE |
| 琥珀酸美托洛尔 | 宜昌东阳光长江药业股份有限公司 | Y20170000556 | A | Exact ingredient | 2026/07/14 | 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.
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2026/09/20Accepted
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2026/09/20Accepted
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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