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Timolol Maleate Eye Drops(马来酸噻吗洛尔滴眼液)

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

Last 90 days: Accepted: 2 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: 33 distinct approval numbers and 25 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
广东众生药业股份有限公司 国药准字H20178006 5ml:25mg(以噻吗洛尔计) Category A (甲) XS01EDS008G010010100371NHSA
天津市中央药业有限公司 国药准字H12020054 5ml:12.5mg Category A (甲) XS01EDS008G010010100928NHSA
亚邦医药股份有限公司 国药准字H32020377 5ml:12.5mg Category A (甲) XS01EDS008G010010101510NHSA
江苏云阳集团药业有限公司 国药准字H32020313 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010101519NHSA
江苏颐海药业有限责任公司 国药准字H32020535 5ml:12.5mg Category A (甲) XS01EDS008G010010101730NHSA
湖北远大天天明制药有限公司 国药准字H20053459 0.4ml:1mg Category A (甲) XS01EDS008G010010101791NHSA
湖北潜江制药股份有限公司 国药准字H20065130 5ml:12.5mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010101840NHSA
湖北远大天天明制药有限公司 国药准字H20045947 5ml:12.5mg Category A (甲) XS01EDS008G010010101967NHSA
武汉五景药业有限公司 国药准字H42021078 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010101978NHSA
成都恒瑞制药有限公司 国药准字H20063099 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010102031NHSA
石家庄格瑞药业有限公司 国药准字H20243071 0.5%(5ml:25mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010010102733NHSA
石家庄四药有限公司 国药准字H20254418 0.25%(0.3ml:0.75mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010010102763NHSA
津药永光(河北)制药有限公司 国药准字H20063920 5ml:25mg Category A (甲) XS01EDS008G010010102817NHSA
开封制药(集团)有限公司 国药准字H20093786 0.25%(5ml:12.5mg,按噻吗洛尔计) Category A (甲) XS01EDS008G010010103139NHSA
长春长庆药业集团有限公司 国药准字H22020431 5ml:25mg Category A (甲) XS01EDS008G010010103299NHSA
山东博士伦福瑞达制药有限公司 国药准字H20023109 5ml:25mg;8ml:40mg;10ml:50mg Category A (甲) XS01EDS008G010010104072NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010104127NHSA
安徽省双科药业有限公司 国药准字H20045418 5ml:25mg Category A (甲) XS01EDS008G010010104335NHSA
合肥立方制药股份有限公司 国药准字H20253876 0.5%(5ml:25mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010010104394NHSA
合肥利民制药有限公司 国药准字H34022763 5ml:25mg Category A (甲) XS01EDS008G010010104423NHSA
宁夏康亚药业股份有限公司 国药准字H20093905 0.25% Category A (甲) XS01EDS008G010010105911NHSA
江苏远恒药业有限公司 国药准字H20249112 0.25%(5ml:12.5mg)(按C13H24N4O3S计) Category A (甲) XS01EDS008G010010106033NHSA
广东宏盈科技有限公司 国药准字H20133308 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010107415NHSA
扬州中宝药业股份有限公司 国药准字H20254927 0.5%(0.3ml:1.5mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010010181161NHSA
天津市中央药业有限公司 国药准字H12020053 5ml:25mg Category A (甲) XS01EDS008G010010200928NHSA
湖北远大天天明制药有限公司 国药准字H20053459 0.4ml:1mg Category A (甲) XS01EDS008G010010201791NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010010204127NHSA
扬州中宝药业股份有限公司 国药准字H20254927 0.5%(0.3ml:1.5mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010010281161NHSA
广东松下药业有限公司 国药准字H44024066 5ml:12.5mg Category A (甲) XS01EDS008G010020100389NHSA
江苏颐海药业有限责任公司 国药准字H32020534 5ml:25mg Category A (甲) XS01EDS008G010020101730NHSA
湖北远大天天明制药有限公司 国药准字H20045948 5ml:25mg Category A (甲) XS01EDS008G010020101967NHSA
武汉新瑞医药科技有限公司 国药准字H20234367 0.5%(5ml:25mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010020101978NHSA
石家庄格瑞药业有限公司 国药准字H20243072 0.25%(5ml:12.5mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010020102733NHSA
石家庄四药有限公司 国药准字H20254432 0.5%(0.3ml:1.5mg,按C₁₃H₂₄N₄O₃S计) Category A (甲) XS01EDS008G010020102763NHSA
山东博士伦福瑞达制药有限公司 国药准字H20023109 5ml:25mg;8ml:40mg;10ml:50mg Category A (甲) XS01EDS008G010020104072NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010020104127NHSA
江苏远恒药业有限公司 国药准字H20249113 0.5%(5ml:25mg)(按C13H24N4O3S计) Category A (甲) XS01EDS008G010020106033NHSA
广东宏盈科技有限公司 国药准字H20133308 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010020107415NHSA
广东松下药业有限公司 国药准字H44024067 5ml:25mg Category A (甲) XS01EDS008G010020200389NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010020204127NHSA
山东博士伦福瑞达制药有限公司 国药准字H20023109 5ml:25mg;8ml:40mg;10ml:50mg Category A (甲) XS01EDS008G010030104072NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010030104127NHSA
广东宏盈科技有限公司 国药准字H20133308 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010030107415NHSA
山东辰欣佛都药业股份有限公司 国药准字H37022028 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010030204127NHSA
广东宏盈科技有限公司 国药准字H20133308 5ml:25mg(按噻吗洛尔计) Category A (甲) XS01EDS008G010040107415NHSA

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 2 distinct first applicants.

Generic 4

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
成都普什制药有限公司 CYHS2602494 Generic2026/10/12Not stated by sourceCDE
成都普什制药有限公司 CYHS2602493 Generic2026/10/12Not stated by sourceCDE
广东南国药业有限公司 CYHS2601324 Generic2026/06/08Not stated by sourceCDE
广东南国药业有限公司 CYHS2502062 Generic2025/06/11Not 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
成都普什制药有限公司 CYHS2602494 Generic2026/10/12Not stated by sourceCDE
成都普什制药有限公司 CYHS2602493 Generic2026/10/12Not stated by sourceCDE
广东南国药业有限公司 CYHS2601324 Generic2026/06/08Not stated by sourceCDE
API registrations

Non-component matches: 7 companies with A status and 3 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
噻吗洛尔半水合物汉瑞药业(荆门)有限公司Y20260000035ISalt-normalized ingredient2026/01/26CDE
马来酸噻吗洛尔PCASY20250000663IExact ingredient2025/11/13CDE
马来酸噻吗洛尔浙江江北南海药业有限公司Y20250000067IExact ingredient2025/05/28CDE
马来酸噻吗洛尔天津民祥药业有限公司Y20230001317AExact ingredient2025/05/20CDE
马来酸噻吗洛尔江苏慈星药业有限公司Y20220001347AExact ingredient2024/01/17CDE
马来酸噻吗洛尔石家庄格瑞药业有限公司Y20220000253AExact ingredient2024/11/05CDE
马来酸噻吗洛尔Fareva La ValleeY20190000119AExact ingredient2024/11/07CDE
马来酸噻吗洛尔天津力生制药股份有限公司Y20190007964AExact ingredient2025/06/28CDE
马来酸噻吗洛尔天津民祥生物医药股份有限公司Y20170002259AExact ingredient2024/05/01CDE
马来酸噻吗洛尔Centaur Pharmaceuticals Private LimitedY20170000577AExact ingredient2024/12/31CDE

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. 2026/10/12Accepted

    成都普什制药有限公司

    CYHS2602494

    Fact date: 2026/10/12 · Site observation date: 2026/10/22

    View source ↗
  2. 2026/10/12Accepted

    成都普什制药有限公司

    CYHS2602493

    Fact date: 2026/10/12 · 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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