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辅酶Q10片

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

Last 90 days: Accepted: 1 application

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: 1 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 1 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
成都倍特药业股份有限公司成都倍特药业股份有限公司 国药准字H20264726 2026/06/10 10mg 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: 4 distinct approval numbers and 4 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
远大医药(中国)有限公司 国药准字H10930021 10mg Not stated by sourceXV02DXF109A001010101693NHSA
黑龙江江世药业有限公司 国药准字H20003414 10mg Not stated by sourceXV02DXF109A001010103740NHSA
浙江三生蔓迪药业有限公司 国药准字H19994099 10mg Not stated by sourceXV02DXF109A001010104726NHSA
黑龙江江世药业有限公司 国药准字H20003414 10mg Not stated by sourceXV02DXF109A001010203740NHSA
浙江三生蔓迪药业有限公司 国药准字H19994099 10mg Not stated by sourceXV02DXF109A001010204726NHSA
黑龙江江世药业有限公司 国药准字H20003414 10mg Not stated by sourceXV02DXF109A001010303740NHSA
成都倍特药业股份有限公司 国药准字H20264726 10mg Not stated by sourceXV02DXF109A001010102013NHSA

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: 7 filings and 7 distinct first applicants.

Generic 7

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
远大医药(仙桃)制药有限公司 CYHS2602347 Generic2026/09/20Not stated by sourceCDE
海南赛立克药业有限公司 CYHS2600988 Generic2026/04/28Not stated by sourceCDE
安徽肽渡生物医药科技有限公司;华益药业科技(安徽)有限公司 CYHS2503886 Generic2025/11/06Not stated by sourceCDE
辽宁鑫善源药业有限公司 CYHS2503760 Generic2025/10/22Not stated by sourceCDE
漯河市汇创医药有限公司;裕松源药业有限公司 CYHS2502621 Generic2025/07/22Not stated by sourceCDE
杭州和泽坤元药业有限公司;浙江皓格药业有限公司 CYHS2502526 Generic2025/07/15Not stated by sourceCDE
海南元盈医药科技有限公司;天津汉瑞药业有限公司 CYHS2501942 Generic2025/05/31Not 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
远大医药(仙桃)制药有限公司 CYHS2602347 Generic2026/09/20Not stated by sourceCDE
海南赛立克药业有限公司 CYHS2600988 Generic2026/04/28Not stated by sourceCDE
API registrations

Non-component matches: 8 companies with A status and 2 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
辅酶Q10黑龙江新和成生物科技有限公司Y20210001158AExact ingredient2026/03/21CDE
辅酶Q10神舟生物科技有限责任公司Y20200001445IExact ingredient2021/01/22CDE
辅酶Q10内蒙古金达威药业有限公司Y20200001329IExact ingredient2021/01/04CDE
辅酶Q10Eisai Co.,Ltd.Y20190009159AExact ingredient—CDE
辅酶Q10玉溪健坤生物药业有限公司Y20190008330AExact ingredient2024/03/19CDE
辅酶Q10浙江新和成股份有限公司Y20190006862AExact ingredient—CDE
辅酶Q10康普药业股份有限公司Y20190005992AExact ingredient—CDE
辅酶Q10天方药业有限公司Y20190003034AExact ingredient—CDE
辅酶Q10浙江医药股份有限公司新昌制药厂Y20190001704AExact ingredient2026/06/25CDE
辅酶Q10KANEKA CORPORATIONY20170001933AExact ingredient2025/07/21CDE

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. 2026/09/20Accepted

    远大医药(仙桃)制药有限公司

    CYHS2602347

    Fact date: 2026/09/20 · Site observation date: 2026/10/22

    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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