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Public drug landscapesDrug landscape

Acetylcysteine Oral Solution(乙酰半胱氨酸口服溶液)

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

Last 90 days: Marketing application approved: 2 applicationsAccepted: 3 applications

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: 0 holders; 0 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
No matching records were found in the currently loaded source data; coverage dates are listed below.

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: 0 distinct approval numbers and 0 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
No matching records were found in the currently loaded source data; coverage dates are listed below.

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: 11 filings and 6 distinct first applicants.

Generic 11

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
四川海梦智森生物制药有限公司;南京海纳制药有限公司 CYHS2504423 Generic2025/12/26Not stated by sourceCDE
四川海梦智森生物制药有限公司;南京海纳制药有限公司 CYHS2504422 Generic2025/12/26Not stated by sourceCDE
四川海梦智森生物制药有限公司;南京海纳制药有限公司 CYHS2504421 Generic2025/12/26Not stated by sourceCDE
葵花药业集团(冀州)有限公司 CYHS2602584 Generic2026/10/21Not stated by sourceCDE
葵花药业集团(冀州)有限公司 CYHS2602583 Generic2026/10/21Not stated by sourceCDE
浙江前进药业有限公司;知和(山东)大药厂有限公司 CYHS2602277 Generic2026/09/15Not stated by sourceCDE
成都柏腾医药科技有限公司;成都倍特得诺药业有限公司 CYHS2504420 Generic2025/12/26Not stated by sourceCDE
九华华源药业股份有限公司;合肥诚志生物制药有限公司 CYHS2503933 Generic2025/11/12Not stated by sourceCDE
九华华源药业股份有限公司;合肥诚志生物制药有限公司 CYHS2503932 Generic2025/11/12Not stated by sourceCDE
合肥国药诺和药业有限公司;合肥诚志生物制药有限公司 CYHS2502130 Generic2025/06/14Not stated by sourceCDE
合肥国药诺和药业有限公司;合肥诚志生物制药有限公司 CYHS2502129 Generic2025/06/14Not stated by sourceCDE
New generic filings in 2026

Loaded records: 3 filings and 2 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
葵花药业集团(冀州)有限公司 CYHS2602584 Generic2026/10/21Not stated by sourceCDE
葵花药业集团(冀州)有限公司 CYHS2602583 Generic2026/10/21Not stated by sourceCDE
浙江前进药业有限公司;知和(山东)大药厂有限公司 CYHS2602277 Generic2026/09/15Not stated by sourceCDE
API registrations

Non-component matches: 12 companies with A status and 5 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
乙酰半胱氨酸浙江海昌药业股份有限公司Y20260000718IExact ingredient2026/08/14CDE
乙酰半胱氨酸PharmaZell GmbHY20250001320IExact ingredient2026/04/28CDE
乙酰半胱氨酸浙江海洲制药股份有限公司Y20260000217IExact ingredient2026/03/27CDE
乙酰半胱氨酸津药药业股份有限公司Y20240001520IExact ingredient2025/05/28CDE
乙酰半胱氨酸湖南九典宏阳制药有限公司Y20240001419AExact ingredient2026/09/10CDE
乙酰半胱氨酸浙江金华康恩贝生物制药有限公司Y20240001287AExact ingredient2026/06/02CDE
乙酰半胱氨酸湖南华纳大药厂手性药物有限公司Y20230001045AExact ingredient2025/05/20CDE
乙酰半胱氨酸浙江诚意药业股份有限公司Y20220000261AExact ingredient2024/05/22CDE
乙酰半胱氨酸七星化学制药股份有限公司Y20220000066AExact ingredient2024/01/25CDE
乙酰半胱氨酸山西阳和药业有限公司Y20210001235AExact ingredient2025/02/06CDE
乙酰半胱氨酸福建南方制药股份有限公司Y20210001183AExact ingredient2024/09/17CDE
乙酰半胱氨酸浙江赛默制药有限公司Y20210001203AExact ingredient2025/10/18CDE
乙酰半胱氨酸Nippon Rika Co., Ltd.Y20200000078AExact ingredient2023/03/24CDE
乙酰半胱氨酸武汉远大弘元股份有限公司Y20190009549AExact ingredient2025/09/24CDE
乙酰半胱氨酸F.I.S. Fabbrica Italiana Sintetici S.P.A.Y20190009052AExact ingredient2024/05/22CDE
乙酰半胱氨酸浙江诚意药业股份有限公司Y20190007528AExact ingredient2024/05/22CDE
乙酰半胱氨酸湖北新生源生物工程有限公司Y20190006101AExact ingredient2026/01/29CDE
乙酰半胱氨酸MOEHS IBERICA S.L.Y20170000715IExact ingredient—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.

  1. 2026/11/03Marketing application approved

    安徽茂康药业有限公司

    CYHS2500605 · 国药准字H20266442

    Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

    The loaded NHSA codes and chemical-drug catalogue contain no evidence confirming an earlier same-name approval for this company. This does not establish the absence of an earlier approval.

    View source · Table row 28 ↗
  2. 2026/11/03Marketing application approved

    舒美奇成都生物科技有限公司

    CYHS2404478 · 国药准字H20266435

    Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

    The loaded NHSA codes and chemical-drug catalogue contain no evidence confirming an earlier same-name approval for this company. This does not establish the absence of an earlier approval.

    View source · Table row 14 ↗
  3. 2026/10/21Accepted

    葵花药业集团(冀州)有限公司

    CYHS2602584

    Fact date: 2026/10/21 · Site observation date: 2026/10/22

    View source ↗
  4. 2026/10/21Accepted

    葵花药业集团(冀州)有限公司

    CYHS2602583

    Fact date: 2026/10/21 · Site observation date: 2026/10/22

    View source ↗
  5. 2026/09/15Accepted

    浙江前进药业有限公司;知和(山东)大药厂有限公司

    CYHS2602277

    Fact date: 2026/09/15 · 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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