药格局YaoGeJu

Public drug landscapesDrug landscape

Sodium Nitroprusside Injection(硝普钠注射液)

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

Follow for free
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 12 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Dr. Reddy’s Laboratories LimitedDr. Reddy’s Laboratories Limited 国药准字HJ20260086 2026/09/29 2ml:50mg[按Na2[Fe(CN)5NO] ·2H2O计] 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
Caplin Steriles LimitedCaplin Steriles Limited 国药准字HJ20260085 2026/09/22 2ml:50mg[按Na2Fe(CN)5NO·2H2O计] 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
山东齐都药业有限公司山东齐都药业有限公司 国药准字H20265876 2026/09/08 2ml:50mg[按Na2Fe(CN)5NO?2H2O计] 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
北京世桥生物制药有限公司北京世桥生物制药有限公司 国药准字H20265595 2026/08/04 2ml︰50mg[按Na2[Fe(CN)5NO]·2H2O计] 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
嘉实(湖南)医药科技有限公司康普药业股份有限公司 国药准字H20264923 2026/06/23 2ml:50mg [按Na2Fe(CN)5NO·2H2O计] 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
华夏生生药业(北京)有限公司华夏生生药业(北京)有限公司 国药准字H20264379 2026/05/19 2ml:50mg[按Na2Fe(CN)5NO·2H2O计] 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
重庆药友制药有限责任公司重庆药友制药有限责任公司 国药准字H20264118 2026/04/21 2ml:50mg[按Na2Fe(CN)5NO·2H2O计] 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
成都瑞尔医药科技有限公司成都市海通药业有限公司 国药准字H20263476 2026/02/25 2ml∶50mg(按Na2[Fe(CN)5NO]·2H2O计) 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
成都新恒创药业有限公司成都新恒创药业有限公司 国药准字H20249215 2024/10/29 2ml:50mg(按Na<sub>2</sub>Fe(CN)<sub>5</sub>NO·2H<sub>2</sub>O计) 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
海南普利制药股份有限公司海南普利制药股份有限公司 国药准字H20223226 2022/04/12 2ml:50mg[按Na2[Fe(CN)5NO] ·2H2O计] 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
湖南恒生制药股份有限公司湖南恒生制药股份有限公司 国药准字H20256405 2025/12/30 2ml:50mg [按Na2Fe(CN)5NO·2H2O计] 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
康普药业股份有限公司康普药业股份有限公司 国药准字H20266289 2026/10/20 2ml:50mg(按Na2Fe(CN)5NO·2H2O计) 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: 10 distinct approval numbers and 10 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
北京世桥生物制药有限公司 国药准字H20265595 2ml:50mg[按Na2Fe(CN)5NO·2H2O计] Category A (甲) XC02DDX070B002010100123NHSA
重庆药友制药有限责任公司 国药准字H20264118 2ml:50mg(按Na₂Fe(CN)₅NO·2H₂O计) Category A (甲) XC02DDX070B002010101066NHSA
山东齐都药业有限公司 国药准字H20265876 2ml:50mg[按Na₂Fe(CN)₅NO·2H₂O计] Category A (甲) XC02DDX070B002010104145NHSA
湖南恒生制药股份有限公司 国药准字H20256405 2ml:50mg [按Na₂Fe(CN)₅NO·2H₂O计] Category A (甲) XC02DDX070B002010104900NHSA
海南普利制药股份有限公司 国药准字H20223226 2ml:50mg[按Na₂[Fe(CN)₅NO]·2H₂O计] Category A (甲) XC02DDX070B002010105801NHSA
成都新恒创药业有限公司 国药准字H20249215 2ml:50mg(按Na₂Fe(CN)₅NO•2H₂O计) Category A (甲) XC02DDX070B002010109552NHSA
华夏生生药业(北京)有限公司 国药准字H20264379 2ml:50mg[按Na₂Fe(CN)₅NO·2H₂O计] Category A (甲) XC02DDX070B002010109910NHSA
嘉实(湖南)医药科技有限公司 国药准字H20264923 2ml:50mg [按Na₂Fe(CN)₅NO·2H₂O计] Category A (甲) XC02DDX070B002010183048NHSA
成都瑞尔医药科技有限公司 国药准字H20263476 2ml:50mg(按Na₂Fe(CN)₅NO·2H₂O计) Category A (甲) XC02DDX070B002010184534NHSA
成都瑞尔医药科技有限公司 国药准字H20263476 2ml:50mg(按Na₂Fe(CN)₅NO·2H₂O计) Category A (甲) XC02DDX070B002010284534NHSA
Caplin Steriles Limited 国药准字HJ20260085 2ml:50mg[按Na₂Fe(CN)₅NO•2H₂O计] Category A (甲) XC02DDX070B002010185310NHSA

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: 15 filings and 14 distinct first applicants.

Generic 15

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
南京海纳制药有限公司 CYHS2503804 Generic2025/10/28Not stated by sourceCDE
扬州中宝药业股份有限公司 CYHS2600947 Generic2026/04/24Not stated by sourceCDE
丹东医创药业有限责任公司 CYHS2602475 Generic2026/10/10Not stated by sourceCDE
上海禾丰制药有限公司 CYHS2503741 Generic2025/10/21Not stated by sourceCDE
四川奇裕医药科技有限公司;康普药业股份有限公司 CYHS2503444 Generic2025/09/18Not stated by sourceCDE
华润双鹤药业股份有限公司 CYHS2503066 Generic2025/08/20Not stated by sourceCDE
四川健林药业有限责任公司;四川科瑞德制药股份有限公司 CYHS2502341 Generic2025/07/02Not stated by sourceCDE
广州世济医药科技有限公司;广东星昊药业有限公司 CYHS2502228 Generic2025/06/20Not stated by sourceCDE
海南倍特药业有限公司 CYHS2502213 Generic2025/06/20Not stated by sourceCDE
仁合益康汇泽药业河北有限公司 CYHS2502175 Generic2025/06/18Not stated by sourceCDE
河北一品制药股份有限公司 CYHS2502011 Generic2025/06/06Not stated by sourceCDE
山东齐都药业有限公司 CYHS2501982 Generic2025/06/05Not stated by sourceCDE
山东齐都药业有限公司 CYHS2501981 Generic2025/06/05Not stated by sourceCDE
海南海和制药有限公司;海南灵康制药有限公司 CYHS2501159 Generic2025/03/25Not stated by sourceCDE
海南爱科制药有限公司;海南灵康制药有限公司 CYHS2500578 Generic2025/02/06Not 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
扬州中宝药业股份有限公司 CYHS2600947 Generic2026/04/24Not stated by sourceCDE
丹东医创药业有限责任公司 CYHS2602475 Generic2026/10/10Not stated by sourceCDE
API registrations

Non-component matches: 17 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
硝普钠湖南复瑞生物医药技术有限责任公司Y20260000486IExact ingredient2026/08/18CDE
硝普钠绪必迪药业(沧州)有限公司Y20250001347IExact ingredient2025/12/15CDE
硝普钠河北安健成益医药科技有限公司Y20250000236AExact ingredient2026/09/11CDE
硝普钠安徽普利药业有限公司Y20240001218AExact ingredient2026/03/26CDE
硝普钠山东川成医药有限公司Y20240000799AExact ingredient2026/10/31CDE
硝普钠双鹤药业(商丘)有限责任公司Y20240000362AExact ingredient2025/08/22CDE
硝普钠湖南恒生制药股份有限公司Y20240000094AExact ingredient2025/08/26CDE
硝普钠Azico Biophore India Pvt LtdY20230001195AExact ingredient2026/08/28CDE
硝普钠河南中帅药业有限公司Y20220001337AExact ingredient2024/09/29CDE
硝普钠成都新恒创药业有限公司Y20220001181AExact ingredient2025/12/20CDE
硝普钠湖南华纳大药厂手性药物有限公司Y20210000083AExact ingredient2026/04/14CDE
硝普钠三门峡赛诺维制药有限公司Y20190009710AExact ingredient2025/03/14CDE
硝普钠湖北葛店人福药业有限责任公司Y20190007504AExact ingredient2025/03/01CDE
硝普钠华润双鹤药业股份有限公司Y20190005092AExact ingredient2025/07/29CDE
硝普钠康普药业股份有限公司Y20190004573AExact ingredient2026/03/21CDE
硝普钠上海迪冉郸城制药有限公司Y20190004349AExact ingredient2024/11/01CDE
硝普钠北京世桥生物制药有限公司Y20190003626AExact ingredient—CDE
硝普钠丹东医创药业有限责任公司Y20190002726AExact ingredient2025/05/22CDE
硝普钠海南普利制药股份有限公司Y20190000020AExact ingredient2024/03/14CDE
硝普钠三门峡赛诺维制药有限公司Y20170002000AExact ingredient2022/10/18CDE
硝普钠河北一品制药股份有限公司Y20260000897IExact ingredient2026/10/30CDE

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. 2026/11/03Marketing application approved

    山西九康医药科技有限公司

    CYHS2501176 · 国药准字H20266490

    Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

    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 45 ↗
  2. 2026/10/31No longer listed under review

    成都欣捷高新技术开发股份有限公司;四川美大康佳乐药业有限公司

    CYHS2501096

    Fact date: 2026/10/31 · Site observation date: 2026/10/31

    Accepted: 2025/03/18

    not on the CDE under-review list in this snapshot; the review / approval outcome is to be checked

    View source ↗
  3. 2026/10/31No longer listed under review

    成都欣捷高新技术开发股份有限公司;四川美大康佳乐药业有限公司

    CYHS2501095

    Fact date: 2026/10/31 · Site observation date: 2026/10/31

    Accepted: 2025/03/18

    not on the CDE under-review list in this snapshot; the review / approval outcome is to be checked

    View source ↗
  4. 2026/10/20Marketing application approved

    中润药业有限公司

    CYHS2501180 · 国药准字H20266312

    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 44 ↗
  5. 2026/10/20Marketing application approved

    康普药业股份有限公司

    CYHS2500903 · 国药准字H20266289

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

    Same-name approval records dated before this approval were found, with company roles identified below:

    • Manufacturer record / approval date · 国药准字H20264923 · 2026/06/23 · View source
    View source · Table row 39 ↗
  6. 2026/10/10Accepted

    丹东医创药业有限责任公司

    CYHS2602475

    Fact date: 2026/10/10 · 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.

Free follow

Follow changes to Sodium Nitroprusside Injection

Up to 3 drugs per email address, in one weekly digest. Starts after email confirmation; unsubscribe at any time.

Confirmation links expire in 7 days. No digest is sent before confirmation; existing follows are not duplicated.