药格局YaoGeJu

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阿仑膦酸钠口服溶液

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: 11 distinct approval numbers and 11 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
广州一品红制药有限公司 国药准字H20263255 75ml∶70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010101012NHSA
山东新华制药股份有限公司 国药准字H20255791 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010104187NHSA
武汉华尔生物科技有限公司 国药准字H20263732 75ml:70mg (按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010106652NHSA
河北仁合益康药业有限公司 国药准字H20265452 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010110349NHSA
秦皇岛爱晖药业有限公司 国药准字H20255508 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010183136NHSA
知和(山东)大药厂有限公司 国药准字H20263425 75ml:70mg(以C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010183686NHSA
湖南普道医药技术有限公司 国药准字H20255909 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010183849NHSA
长春澜江医药科技有限公司 国药准字H20255910 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010183864NHSA
珠海北杉生物科技有限公司 国药准字H20263672 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010184470NHSA
湖北欣泽霏药业有限公司 国药准字H20264488 75ml:70mg(以C₄H₁₃NO₇P₂ 计) Not stated by sourceXM05BAA029X001010184522NHSA
海南斯达制药有限公司 国药准字H20265874 75ml:70mg(按C₄H₁₃NO₇P₂计) Not stated by sourceXM05BAA029X001010105816NHSA

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: 7 filings and 7 distinct first applicants.

Generic 7

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
北京海晶生物医药科技有限公司;安徽永生堂药业有限责任公司 CYHS2600916 Generic2026/04/22Not stated by sourceCDE
北京双鹭药业股份有限公司 CYHS2600709 Generic2026/03/24Not stated by sourceCDE
陕西新沣华生物科技有限公司;陕西汉江药业集团股份有限公司 CYHS2504172 Generic2025/12/05Not stated by sourceCDE
北京民康百草医药科技有限公司;湖南九典制药股份有限公司 CYHS2502869 Generic2025/08/08Not stated by sourceCDE
黑龙江中桂制药有限公司 CYHS2501120 Generic2025/03/20Not stated by sourceCDE
西洲医药科技(浙江)有限公司;浙江北生药业汉生制药有限公司 CYHS2602600 Generic2026/10/22Not stated by sourceCDE
江苏贝佳制药有限公司 CYHS2602641 Generic2026/10/29Not 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
北京海晶生物医药科技有限公司;安徽永生堂药业有限责任公司 CYHS2600916 Generic2026/04/22Not stated by sourceCDE
北京双鹭药业股份有限公司 CYHS2600709 Generic2026/03/24Not stated by sourceCDE
西洲医药科技(浙江)有限公司;浙江北生药业汉生制药有限公司 CYHS2602600 Generic2026/10/22Not stated by sourceCDE
江苏贝佳制药有限公司 CYHS2602641 Generic2026/10/29Not stated by sourceCDE
API registrations

Non-component matches: 11 companies with A status and 2 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
阿仑膦酸钠Divi's Laboratories LimitedY20260000059IExact ingredient2026/07/22CDE
阿仑膦酸钠南京九霄药业有限公司Y20250000219AExact ingredient2026/08/25CDE
阿仑膦酸钠PHARMACEUTICAL WORKS POLPHARMA S.A.Y20220000174AExact ingredient2026/08/12CDE
阿仑膦酸钠陕西汉江药业集团股份有限公司Y20190009556AExact ingredient2025/10/12CDE
阿仑膦酸钠海南中和药业股份有限公司Y20190006203AExact ingredient2024/07/11CDE
阿仑膦酸钠海南海神同洲制药有限公司Y20190004386AExact ingredient2024/07/05CDE
阿仑膦酸钠海南益尔药业有限公司Y20190004283AExact ingredient2024/08/01CDE
阿仑膦酸钠石药集团欧意药业有限公司Y20190003357AExact ingredient2024/05/29CDE
阿仑膦酸钠北京福元医药股份有限公司Y20190003085AExact ingredient2025/01/18CDE
阿仑膦酸钠扬子江药业集团江苏海慈生物药业有限公司Y20190002714AExact ingredient2025/03/27CDE
阿仑膦酸钠杭州澳医保灵药业有限公司Y20190001315AExact ingredient—CDE
阿仑膦酸钠陕西汉江药业集团股份有限公司Y20180000234IExact ingredient2019/04/29CDE
阿仑膦酸钠绍兴民生医药股份有限公司Y20170000812AExact ingredient2024/08/02CDE

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. 2026/10/29Accepted

    江苏贝佳制药有限公司

    CYHS2602641

    Fact date: 2026/10/29 · Site observation date: 2026/10/30

    View source ↗
  2. 2026/10/22Accepted

    西洲医药科技(浙江)有限公司;浙江北生药业汉生制药有限公司

    CYHS2602600

    Fact date: 2026/10/22 · Site observation date: 2026/10/23

    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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