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MOVICOL Ready To Take Sachet, Powder For Oral Solution(复方聚乙二醇(3350)电解质口服溶液)

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

Last 90 days: Marketing application approved: 1 applicationAccepted: 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: 7 distinct approval numbers and 7 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
广州一品红制药有限公司 国药准字H20265982 25ml/袋 Not stated by sourceXA06ADF336X001010101012NHSA
葵花药业集团(唐山)生物制药有限公司 国药准字H20263376 25ml/袋 Not stated by sourceXA06ADF336X001010102798NHSA
广西维威制药有限公司 国药准字H20263335 25ml/袋 Not stated by sourceXA06ADF336X001010105237NHSA
江苏开元药业有限公司 国药准字H20265869 25ml/袋 Not stated by sourceXA06ADF336X001010183955NHSA
重庆迈川医药科技有限公司 国药准字H20253653 25ml/袋 Not stated by sourceXA06ADF336X001010184196NHSA
重庆迈川医药科技有限公司 国药准字H20253653 25ml/袋 Not stated by sourceXA06ADF336X001010284196NHSA
舒泰神(北京)生物制药股份有限公司 国药准字H20223679 25ml/袋 Not stated by sourceXA06ADF336X001010100233NHSA
浙江远力健药业有限责任公司 国药准字H20243831 25ml/袋 Not stated by sourceXA06ADF336X001010109207NHSA
浙江远力健药业有限责任公司 国药准字H20243831 25ml/袋 Not stated by sourceXA06ADF336X001010209207NHSA
浙江远力健药业有限责任公司 国药准字H20243831 25ml/袋 Not stated by sourceXA06ADF336X001010309207NHSA

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: 16 filings and 16 distinct first applicants.

Generic 16

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
江苏神华药业有限公司 CYHS2600417 Generic2026/02/10Not stated by sourceCDE
湖北多瑞药业有限公司;浙江国镜药业有限公司 CYHS2602564 Generic2026/10/19Not stated by sourceCDE
沈阳达善医药科技有限公司;辽宁大熊制药有限公司 CYHS2601634 Generic2026/07/08Not stated by sourceCDE
北京圣永制药有限公司 CYHS2600584 Generic2026/02/28Not stated by sourceCDE
杭州呋欧医药科技有限公司;浙江凯润药业股份有限公司 CYHS2504121 Generic2025/12/02Not stated by sourceCDE
杭州民生药物研究院有限公司;四川先通药业有限责任公司 CYHS2503990 Generic2025/11/18Not stated by sourceCDE
赤峰源生药业有限公司 CYHS2503955 Generic2025/11/14Not stated by sourceCDE
河北东圣科宇医药科技有限公司;安徽永生堂药业有限责任公司 CYHS2503749 Generic2025/10/21Not stated by sourceCDE
北京诚济制药股份有限公司 CYHS2503692 Generic2025/10/16Not stated by sourceCDE
河北华晨药业集团有限公司 CYHS2503175 Generic2025/08/29Not stated by sourceCDE
四川奇裕医药科技有限公司;四川先通药业有限责任公司 CYHS2503045 Generic2025/08/19Not stated by sourceCDE
湖北午时药业股份有限公司 CYHS2502957 Generic2025/08/13Not stated by sourceCDE
海南斯达制药有限公司 CYHS2502333 Generic2025/07/02Not stated by sourceCDE
重庆万霖生物医药科技有限公司;安徽永生堂药业有限责任公司 CYHS2502273 Generic2025/06/25Not stated by sourceCDE
安徽四环科宝制药有限公司 CYHS2501766 Generic2025/05/15Not stated by sourceCDE
海南广升誉制药有限公司;华益泰康药业股份有限公司 CYHS2500631 Generic2025/02/08Not stated by sourceCDE
New generic filings in 2026

Loaded records: 4 filings and 4 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
江苏神华药业有限公司 CYHS2600417 Generic2026/02/10Not stated by sourceCDE
湖北多瑞药业有限公司;浙江国镜药业有限公司 CYHS2602564 Generic2026/10/19Not stated by sourceCDE
沈阳达善医药科技有限公司;辽宁大熊制药有限公司 CYHS2601634 Generic2026/07/08Not stated by sourceCDE
北京圣永制药有限公司 CYHS2600584 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. 2026/10/20Marketing application approved

    澳诺(中国)制药有限公司

    CYHS2501587 · 国药准字H20266318

    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 56 ↗
  2. 2026/10/19Accepted

    湖北多瑞药业有限公司;浙江国镜药业有限公司

    CYHS2602564

    Fact date: 2026/10/19 · 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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