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Baloxavir Marboxil Tablets(玛巴洛沙韦片)

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: 3 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 3 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
浙江普利药业有限公司浙江普利药业有限公司 国药准字H20263286 2026/01/27 40mg 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
浙江普利药业有限公司浙江普利药业有限公司 国药准字H20263285 2026/01/27 20mg 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
郑州泰丰制药有限公司郑州泰丰制药有限公司 国药准字H20253114 2025/01/08 20mg 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
石药集团欧意药业有限公司石药集团欧意药业有限公司 国药准字H20223746 2022/10/11 20mg 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: 2 distinct approval numbers and 1 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Roche Pharma(Schweiz) AG 国药准字HJ20210027 20mg Category B (乙) XJ05AXM176A001010182682NHSA
Roche Pharma(Schweiz) AG 国药准字HJ20210028 40mg Category B (乙) XJ05AXM176A001020182682NHSA

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: 12 filings and 8 distinct first applicants.

Generic 12

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
常州制药厂有限公司 CYHS2501820 Generic2025/05/20Not stated by sourceCDE
常州制药厂有限公司 CYHS2501819 Generic2025/05/20Not stated by sourceCDE
江苏德源药业股份有限公司 CYHS2504408 Generic2025/12/26Not stated by sourceCDE
杭州民生药业股份有限公司 CYHS2601781 Generic2026/07/24Not stated by sourceCDE
湘北威尔曼制药股份有限公司 CYHS2601297 Generic2026/06/04Not stated by sourceCDE
湘北威尔曼制药股份有限公司 CYHS2601296 Generic2026/06/04Not stated by sourceCDE
湖南明瑞制药股份有限公司 CYHS2600002 Generic2026/01/05Not stated by sourceCDE
湖南明瑞制药股份有限公司 CYHS2600001 Generic2026/01/05Not stated by sourceCDE
重庆莱美药业股份有限公司;重庆博腾药业有限公司 CYHS2504401 Generic2025/12/25Not stated by sourceCDE
远大医药(湖北)有限公司;远大医药(中国)有限公司 CYHS2503574 Generic2025/09/29Not stated by sourceCDE
九洲生物医药(台州)有限公司 CYHS2502794 Generic2025/08/02Not stated by sourceCDE
九洲生物医药(台州)有限公司 CYHS2502793 Generic2025/08/02Not stated by sourceCDE
New generic filings in 2026

Loaded records: 5 filings and 3 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
杭州民生药业股份有限公司 CYHS2601781 Generic2026/07/24Not stated by sourceCDE
湘北威尔曼制药股份有限公司 CYHS2601297 Generic2026/06/04Not stated by sourceCDE
湘北威尔曼制药股份有限公司 CYHS2601296 Generic2026/06/04Not stated by sourceCDE
湖南明瑞制药股份有限公司 CYHS2600002 Generic2026/01/05Not stated by sourceCDE
湖南明瑞制药股份有限公司 CYHS2600001 Generic2026/01/05Not stated by sourceCDE
API registrations

Non-component matches: 9 companies with A status and 12 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
玛巴洛沙韦山东新时代药业有限公司Y20260000672IExact ingredient2026/08/31CDE
玛巴洛沙韦Shionogi & Co., Ltd.Y20260000559IExact ingredient2026/08/18CDE
玛巴洛沙韦浙江永宁药业股份有限公司Y20260000454IExact ingredient2026/07/30CDE
玛巴洛沙韦河北华晨药业集团有限公司Y20260000464IExact ingredient2026/06/16CDE
玛巴洛沙韦精华制药集团南通有限公司Y20260000203IExact ingredient2026/04/15CDE
玛巴洛沙韦福建南方制药股份有限公司Y20250001326IExact ingredient2026/03/26CDE
玛巴洛沙韦四川泰恩康制药有限公司Y20260000101IExact ingredient2026/03/19CDE
玛巴洛沙韦湖南欧亚药业有限公司Y20260000178IExact ingredient2026/03/18CDE
玛巴洛沙韦湘北威尔曼制药股份有限公司Y20260000150IExact ingredient2026/03/10CDE
玛巴洛沙韦浙江普洛康裕制药有限公司Y20250001470IExact ingredient2026/01/06CDE
玛巴洛沙韦金鸿药业股份有限公司Y20250001186IExact ingredient2025/11/13CDE
玛巴洛沙韦山东诚汇双达药业有限公司Y20250001001IExact ingredient2025/09/24CDE
玛巴洛沙韦黑龙江珍宝岛药业股份有限公司鸡西分公司Y20250000333AExact ingredient2026/11/05CDE
玛巴洛沙韦东北制药集团股份有限公司Y20250000151AExact ingredient2026/07/20CDE
玛巴洛沙韦重庆博腾制药科技股份有限公司Y20250000045AExact ingredient2026/09/29CDE
玛巴洛沙韦安徽艾立德制药有限公司Y20240001330AExact ingredient2026/07/13CDE
玛巴洛沙韦河北国龙制药有限公司Y20240001563AExact ingredient2026/09/29CDE
玛巴洛沙韦湖南明瑞制药股份有限公司Y20240001437AExact ingredient2026/10/23CDE
玛巴洛沙韦江苏德源药业股份有限公司Y20240001428AExact ingredient2026/07/16CDE
玛巴洛沙韦南通常佑药业科技有限公司Y20220000381AExact ingredient2024/02/27CDE
玛巴洛沙韦石药集团欧意药业有限公司Y20210000518AExact ingredient2022/10/20CDE

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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