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Probucol Tablets(普罗布考片)

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

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
齐鲁制药有限公司齐鲁制药有限公司 国药准字H20237019 2023/02/10 0.25g Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) 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: 3 distinct approval numbers and 2 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
颈复康药业集团有限公司 国药准字H10960161 0.25g Category B (乙) XC10AXP096A001010102569NHSA
齐鲁制药有限公司 国药准字H10980054 0.125g Category B (乙) XC10AXP096A001010104021NHSA
颈复康药业集团有限公司 国药准字H10960161 0.25g Category B (乙) XC10AXP096A001010202569NHSA
颈复康药业集团有限公司 国药准字H10960161 0.25g Category B (乙) XC10AXP096A001010402569NHSA
齐鲁制药有限公司 国药准字H20237019 0.25g Category B (乙) XC10AXP096A001020104021NHSA

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 4 distinct first applicants.

Generic 4

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
浙江江北药业有限公司 CYHS2601948 Generic2026/08/10Not stated by sourceCDE
宁夏康亚药业股份有限公司 CYHS2601226 Generic2026/06/01Not stated by sourceCDE
山西华夏泰康医药集团有限公司;浙江普利药业有限公司 CYHS2600190 Generic2026/01/16Not stated by sourceCDE
北京福元医药股份有限公司 CYHS2600014 Generic2026/01/05Not stated by sourceCDE
New generic filings in 2026

Loaded records: 4 filings and 4 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
浙江江北药业有限公司 CYHS2601948 Generic2026/08/10Not stated by sourceCDE
宁夏康亚药业股份有限公司 CYHS2601226 Generic2026/06/01Not stated by sourceCDE
山西华夏泰康医药集团有限公司;浙江普利药业有限公司 CYHS2600190 Generic2026/01/16Not stated by sourceCDE
北京福元医药股份有限公司 CYHS2600014 Generic2026/01/05Not stated by sourceCDE
API registrations

Non-component matches: 2 companies with A status and 7 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
普罗布考河北万岁药业有限公司Y20260000512IExact ingredient2026/06/23CDE
普罗布考石家庄格瑞药业有限公司Y20260000346IExact ingredient2026/05/20CDE
普罗布考天科(荆州)制药有限公司Y20250001468IExact ingredient2026/01/05CDE
普罗布考河北广祥制药有限公司Y20250001260IExact ingredient2025/11/27CDE
普罗布考江苏德源药业股份有限公司Y20250001197IExact ingredient2025/11/12CDE
普罗布考旭富制药科技股份有限公司桃园厂Y20230001077IExact ingredient2025/06/04CDE
普罗布考山东安弘制药有限公司Y20190006841AExact ingredient2026/10/23CDE
普罗布考武邑慈航药业有限公司Y20190005301AExact ingredient2025/01/17CDE
普罗布考浙江京圣药业有限公司Y20260000931IExact ingredient2026/11/09CDE

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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