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聚乙二醇钠钾散

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

Last 90 days: Accepted: 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: 12 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 11 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
湖北唯森制药有限公司湖北唯森制药有限公司 国药准字H20265529 2026/08/04 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 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H20265077 2026/07/08 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 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
河北智恒医药科技股份有限公司石家庄龙泽制药股份有限公司 国药准字H20264724 2026/06/10 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
海南紫程众投生物科技有限公司南京海纳制药有限公司 国药准字H20256496 2025/12/30 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
湖南华纳大药厂股份有限公司湖南华纳大药厂股份有限公司 国药准字H20255590 2025/09/30 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
雅安迅康药业有限公司四川科伦药业股份有限公司 国药准字H20255267 2025/09/02 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
南京海纳制药有限公司南京海纳制药有限公司 国药准字H20254981 2025/07/29 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
四川科伦药业股份有限公司四川科伦药业股份有限公司 国药准字H20254806 2025/07/08 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
广东赛康制药厂有限公司广东赛康制药厂有限公司 国药准字H20253569 2025/03/11 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceCDE
圣嘉(滨海)生物医药科技有限公司江苏欧歌制药有限公司 国药准字H20253326 2025/01/24 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
浙江国镜药业有限公司浙江国镜药业有限公司 国药准字H20253275 2025/01/24 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g 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
山东新华鲁抗医药有限公司山东鲁抗医药集团赛特有限责任公司 国药准字H20249734 2024/12/17 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 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: 13 distinct approval numbers and 12 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
郑州泰丰制药有限公司 国药准字H20265077 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 Not stated by sourceXA06ADJ165P001010107011NHSA
四川信拓医药技术有限公司 国药准字H20264499 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯 化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010184023NHSA
四川信拓医药技术有限公司 国药准字H20264499 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯 化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010284023NHSA
四川信拓医药技术有限公司 国药准字H20264499 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯 化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001020184023NHSA
重庆希尔安药业有限公司 国药准字H20256007 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 Not stated by sourceXA06ADJ165P001010101061NHSA
四川科伦药业股份有限公司 国药准字H20254806 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010102180NHSA
浙江国镜药业有限公司 国药准字H20253275 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010104634NHSA
广东赛康制药厂有限公司 国药准字H20253569 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010180463NHSA
南京海纳制药有限公司 国药准字H20254981 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010180537NHSA
雅安迅康药业有限公司 国药准字H20255267 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010182047NHSA
海南紫程众投生物科技有限公司 国药准字H20256496 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010184112NHSA
圣嘉(滨海)生物医药科技有限公司 国药准字H20253326 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010184450NHSA
重庆希尔安药业有限公司 国药准字H20256007 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g。 Not stated by sourceXA06ADJ165P001010201061NHSA
广东赛康制药厂有限公司 国药准字H20253569 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010280463NHSA
海南紫程众投生物科技有限公司 国药准字H20256496 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010284112NHSA
圣嘉(滨海)生物医药科技有限公司 国药准字H20253326 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010284450NHSA
广东赛康制药厂有限公司 国药准字H20253569 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010380463NHSA
圣嘉(滨海)生物医药科技有限公司 国药准字H20253326 本品为复方制剂,每包含聚乙二醇 3350为13.1250g、氯化钠0.3507g、氯化钾0.0466g、碳酸氢钠0.1785g Not stated by sourceXA06ADJ165P001010384450NHSA
Bridging Pharma Limited 国药准字J20171022 13.8g/包 Not stated by sourceXA06ADJ165P001010106681NHSA
Bridging Pharma Limited 国药准字HJ20170101 13.8g/包 Not stated by sourceXA06ADJ165P001010181734NHSA
山东新华鲁抗医药有限公司 国药准字H20249734 本品为复方制剂,每包含聚乙二醇3350为13.1250g、氯化钠 Not stated by sourceXA06ADJ165P001010183530NHSA
Bridging Pharma Limited 国药准字HJ20170101 13.8g/包 Not stated by sourceXA06ADJ165P001010281734NHSA

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.

Supplement 1 · Generic 2

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Bridging Pharma Limited;Norgine Limited JYHB2600491 Supplement2026/08/25Not stated by sourceCDE
笛卡尔药业(哈尔滨)有限公司;哈尔滨三三药业有限公司 CYHS2600675 Generic2026/03/19Not stated by sourceCDE
宏越科技(湖州)有限公司;杭州仟源保灵药业有限公司 CYHS2600579 Generic2026/02/28Not 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
笛卡尔药业(哈尔滨)有限公司;哈尔滨三三药业有限公司 CYHS2600675 Generic2026/03/19Not stated by sourceCDE
宏越科技(湖州)有限公司;杭州仟源保灵药业有限公司 CYHS2600579 Generic2026/02/28Not stated by sourceCDE
API registrations

Non-component matches: 0 companies with A status and 0 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
No matching records were found in the currently loaded source data; coverage dates are listed below.

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. 2026/08/25Accepted

    Bridging Pharma Limited;Norgine Limited

    JYHB2600491

    Fact date: 2026/08/25 · 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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