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Doxazosin Mesylate Extended Release Tablets(甲磺酸多沙唑嗪缓释片)

Companies, stages and changes, with each record available on this page.

No changes recorded by this site in the last 90 days
Complete CDE snapshot: 2026/11/10 07:27

Current coverage may be incomplete

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Complete CDE snapshot
2026/11/10 07:27
Matching scope
Same generic name; dosage forms and combinations kept separate

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.

Chemical-drug catalogue

Loaded records: 11 holders; 1 in the quality-and-efficacy consistency-evaluation category, and 9 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
河南福森药业有限公司淄博万杰制药有限公司 国药准字H20265126 2026/07/08 4mg(按C23H25N5O5计) 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
石家庄四药有限公司石家庄四药有限公司 国药准字H20264172 2026/04/29 4mg(按C23H25N5O5计) 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
合肥华方医药科技有限公司合肥思普瑞药业有限公司 国药准字H20263175 2026/01/20 4mg(按C23H25N5O5计) 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
南京易亨制药有限公司南京易亨制药有限公司 国药准字H20254756 2025/06/30 4mg(以C23H25N5O5计) 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
四川科伦药业股份有限公司四川科伦药业股份有限公司 国药准字H20253807 2025/04/01 4mg(按C23H25N5O5计) 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
天津力生制药股份有限公司天津力生制药股份有限公司 国药准字H20244353 2024/06/28 4mg(以C23H25N5O5计) 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
华润双鹤利民药业(济南)有限公司华润双鹤利民药业(济南)有限公司 国药准字H20243226 2024/02/23 4mg(以C23H25N5O5计) 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
合肥立方制药股份有限公司合肥立方制药股份有限公司 国药准字H20103571 2023/12/13 4mg(以C23H25N5O5计) Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
乐普制药科技有限公司乐普制药科技有限公司 国药准字H20233964 2023/07/25 4mg(按C23H25O5N5计) 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
江西山香药业有限公司江西山香药业有限公司 国药准字H20233967 2023/07/25 4mg(按C23H25N5O5计) 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
Pfizer Pharma PFE GmbHPfizer Pharmaceuticals LLC H20170174;H20170175 2001/06/29 4mg Imported originator drug (进口原研药品) 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: 12 distinct approval numbers and 12 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
天津力生制药股份有限公司 国药准字H20244353 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010100886NHSA
南京易亨制药有限公司 国药准字H20254756 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010101605NHSA
四川科伦药业股份有限公司 国药准字H20253807 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010102180NHSA
石家庄四药有限公司 国药准字H20264172 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010102763NHSA
河南福森药业有限公司 国药准字H20265126 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010103020NHSA
华润双鹤利民药业(济南)有限公司 国药准字H20243226 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010103973NHSA
合肥立方制药股份有限公司 国药准字H20103571 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010104394NHSA
江西山香药业有限公司 国药准字H20233967 4mg(按C23H25N5O5计) Category B (乙) XC02CAD177A010010105345NHSA
Pfizer Pharma PFE GmbH 国药准字J20140130 4mg Category B (乙) XC02CAD177A010010178715NHSA
乐普制药科技有限公司 国药准字H20233964 4mg(按C₂₃H₂₅O₅N₅计) Category B (乙) XC02CAD177A010010182919NHSA
合肥华方医药科技有限公司 国药准字H20263175 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010183480NHSA
南京易亨制药有限公司 国药准字H20254756 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010201605NHSA
石家庄四药有限公司 国药准字H20264172 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010202763NHSA
华润双鹤利民药业(济南)有限公司 国药准字H20243226 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010203973NHSA
江西山香药业有限公司 国药准字H20233967 4mg(按C23H25N5O5计) Category B (乙) XC02CAD177A010010205345NHSA
Viatris Pharma GmbH 国药准字HJ20170175 4mg Category B (乙) XC02CAD177A010010278715NHSA
乐普制药科技有限公司 国药准字H20233964 4mg(按C₂₃H₂₅O₅N₅计) Category B (乙) XC02CAD177A010010282919NHSA
南京易亨制药有限公司 国药准字H20254756 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010301605NHSA
华润双鹤利民药业(济南)有限公司 国药准字H20243226 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010303973NHSA
江西山香药业有限公司 国药准字H20233967 4mg(按C23H25N5O5计) Category B (乙) XC02CAD177A010010305345NHSA
乐普制药科技有限公司 国药准字H20233964 4mg(按C₂₃H₂₅O₅N₅计) Category B (乙) XC02CAD177A010010382919NHSA
南京易亨制药有限公司 国药准字H20254756 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010401605NHSA
华润双鹤利民药业(济南)有限公司 国药准字H20243226 4mg(以C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010010403973NHSA
合肥立方制药股份有限公司 国药准字H20103571 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010020104394NHSA
乐普制药科技有限公司 国药准字H20233964 4mg(按C₂₃H₂₅O₅N₅计) Category B (乙) XC02CAD177A010020182919NHSA
合肥华方医药科技有限公司 国药准字H20263175 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010020183480NHSA
合肥立方制药股份有限公司 国药准字H20103571 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010020204394NHSA
合肥立方制药股份有限公司 国药准字H20103571 4mg(按C₂₃H₂₅N₅O₅计) Category B (乙) XC02CAD177A010030104394NHSA

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: 3 filings and 3 distinct first applicants.

Generic 3

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
常州制药厂有限公司 CYHS2502476 Generic2025/07/11Not stated by sourceCDE
晖致制药(大连)有限公司 CYHS2600416 Generic2026/02/10Not stated by sourceCDE
上海信谊百路达药业有限公司 CYHS2600147 Generic2026/01/13Not stated by sourceCDE
New generic filings in 2026

Loaded records: 2 filings and 2 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
晖致制药(大连)有限公司 CYHS2600416 Generic2026/02/10Not stated by sourceCDE
上海信谊百路达药业有限公司 CYHS2600147 Generic2026/01/13Not stated by sourceCDE
API registrations

Non-component matches: 14 companies with A status and 1 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
甲磺酸多沙唑嗪Nifty Labs Private LimitedY20250001113IExact ingredient2025/10/29CDE
甲磺酸多沙唑嗪Viatris Pharma GmbHY20230001002AExact ingredient2026/02/24CDE
甲磺酸多沙唑嗪河北国龙制药有限公司Y20220000910AExact ingredient2026/01/28CDE
甲磺酸多沙唑嗪Apitoria Pharma Private LimitedY20210000707AExact ingredient2025/12/12CDE
甲磺酸多沙唑嗪合肥立方制药股份有限公司Y20220000380AExact ingredient2026/07/16CDE
甲磺酸多沙唑嗪'Srini Pharmaceuticals Private LimitedY20200000857AExact ingredient2023/02/23CDE
甲磺酸多沙唑嗪浙江乐普药业股份有限公司Y20190007511AExact ingredient2024/02/05CDE
甲磺酸多沙唑嗪宜宾红光制药厂Y20190005693AExact ingredient—CDE
甲磺酸多沙唑嗪康美药业股份有限公司Y20190003931AExact ingredient—CDE
甲磺酸多沙唑嗪常州制药厂有限公司Y20190003560AExact ingredient2025/05/07CDE
甲磺酸多沙唑嗪涛生制药有限公司Y20190003173AExact ingredient—CDE
甲磺酸多沙唑嗪天方药业有限公司Y20190003031AExact ingredient—CDE
甲磺酸多沙唑嗪浙江金华康恩贝生物制药有限公司Y20190002529AExact ingredient—CDE
甲磺酸多沙唑嗪浙江迪耳药业有限公司Y20190002528AExact ingredient2025/04/22CDE
甲磺酸多沙唑嗪浙江新赛科药业有限公司Y20170000552AExact ingredient2024/05/06CDE
甲磺酸多沙唑嗪合肥立方制药股份有限公司Y20170000322AExact ingredient2024/03/15CDE

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.

  1. No matching records were found in the currently loaded source data; coverage dates are listed below.

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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