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Fexofenadine Hydrochloride Oral Suspension(盐酸非索非那定口服混悬液)

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

Last 90 days: Marketing application approved: 4 applicationsAccepted: 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: 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: 4 distinct approval numbers and 4 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
广州南新制药有限公司 国药准字H20249766 120ml: 0.72g Not stated by sourceXR06AXF024X002010100407NHSA
葵花药业集团重庆小葵花儿童制药有限公司 国药准字H20255183 120ml:0.72g Not stated by sourceXR06AXF024X002010100972NHSA
广州一品红制药有限公司 国药准字H20266079 120ml:0.72g Not stated by sourceXR06AXF024X002010101012NHSA
浙江普利药业有限公司 国药准字H20254473 120ml:0.72g Not stated by sourceXR06AXF024X002010182922NHSA

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
亚宝药业四川制药有限公司 CYHS2602547 Generic2026/10/14Not stated by sourceCDE
桂林华信制药有限公司 CYHS2600563 Generic2026/02/27Not stated by sourceCDE
杭州泓友医药科技有限公司;成都硕德药业有限公司 CYHS2503082 Generic2025/08/22Not 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
亚宝药业四川制药有限公司 CYHS2602547 Generic2026/10/14Not stated by sourceCDE
桂林华信制药有限公司 CYHS2600563 Generic2026/02/27Not stated by sourceCDE
API registrations

Non-component matches: 17 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
盐酸非索非那定M/s. Morepen Laboratories LtdY20240001525IExact ingredient2025/03/05CDE
盐酸非索非那定Chemeca Drugs Private LimitedY20230000849AExact ingredient2026/10/15CDE
盐酸非索非那定Vasudha Pharma Chem Ltd.Y20220001219AExact ingredient2025/08/06CDE
盐酸非索非那定西安万隆制药股份有限公司Y20220000912AExact ingredient2024/06/07CDE
盐酸非索非那定Ind-Swift Laboratories LimitedY20190009263AExact ingredient2023/08/10CDE
盐酸非索非那定Synthimed Labs Private LimitedY20190009262AExact ingredient2026/08/11CDE
盐酸非索非那定浙江乐普药业股份有限公司Y20190007452AExact ingredient2024/02/28CDE
盐酸非索非那定浙江华海药业股份有限公司Y20190007370AExact ingredient2023/07/18CDE
盐酸非索非那定海南沙汀宁制药有限公司Y20190007145AExact ingredient—CDE
盐酸非索非那定北京福元医药股份有限公司Y20190007111AExact ingredient2023/03/24CDE
盐酸非索非那定万特制药(海南)有限公司Y20190006884AExact ingredient2023/03/24CDE
盐酸非索非那定四川省旭晖制药有限公司Y20190006660AExact ingredient—CDE
盐酸非索非那定重庆植恩药业有限公司Y20190006653AExact ingredient—CDE
盐酸非索非那定池州东升药业有限公司Y20190006585AExact ingredient2026/04/20CDE
盐酸非索非那定江苏天士力帝益药业有限公司Y20190006077AExact ingredient2025/08/22CDE
盐酸非索非那定江苏恒瑞医药股份有限公司Y20190004696AExact ingredient2025/08/01CDE
盐酸非索非那定太极集团重庆涪陵制药厂有限公司Y20190004565AExact ingredient2025/02/06CDE
盐酸非索非那定Virupaksha Organics LtdY20170000127AExact ingredient2026/08/07CDE

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. 2026/10/20Marketing application approved

    欧彼乐健康科技(上海)有限公司

    JXHS2500028 · 国药准字HJ20260091

    Fact date: 2026/10/20 · Publication date: 2026/10/22 · Site observation date: 2026/11/03

    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 105 ↗
  2. 2026/10/20Marketing application approved

    欧彼乐健康科技(上海)有限公司

    JXHS2500027 · 国药准字HJ20260090

    Fact date: 2026/10/20 · Publication date: 2026/10/22 · Site observation date: 2026/11/03

    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 104 ↗
  3. 2026/10/20Marketing application approved

    欧彼乐健康科技(上海)有限公司

    JXHS2500021 · 国药准字HJ20260091

    Fact date: 2026/10/20 · Publication date: 2026/10/22 · Site observation date: 2026/11/03

    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 103 ↗
  4. 2026/10/20Marketing application approved

    欧彼乐健康科技(上海)有限公司

    JXHS2500020 · 国药准字HJ20260090

    Fact date: 2026/10/20 · Publication date: 2026/10/22 · Site observation date: 2026/11/03

    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 102 ↗
  5. 2026/10/14Accepted

    亚宝药业四川制药有限公司

    CYHS2602547

    Fact date: 2026/10/14 · 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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