药格局YaoGeJu

Public drug landscapesDrug landscape

Betamethasone Sodium Phosphate Injection(倍他米松磷酸钠注射液)

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

Last 90 days: Accepted: 1 applicationNo longer listed under review: 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: 25 holders; 2 in the quality-and-efficacy consistency-evaluation category, and 22 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
河南利华制药有限公司河南润弘制药股份有限公司 国药准字H20265964 2026/09/15 1ml:4mg(按C22H29FO5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
安徽美来药业股份有限公司河南科伦药业有限公司 国药准字H20265447 2026/08/04 1ml:4mg(按C22H29FO5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
四川美大康华康药业有限公司四川美大康华康药业有限公司 国药准字H20264484 2026/05/19 1ml:4mg(按C22H29FO5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
重庆市义力医药科技有限公司新乡市常乐制药有限责任公司 国药准字H20263689 2026/03/25 1ml:4mg(按C22H29FO5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
云南龙海天然植物药业有限公司西南药业股份有限公司 国药准字H20263606 2026/03/17 1ml∶4mg(按C22H29FO5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
吉林省辉南长龙生化药业股份有限公司吉林省辉南长龙生化药业股份有限公司 国药准字H20263541 2026/03/10 1ml∶4mg(按C22H29FO5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
浙江浙北药业有限公司浙江仙琚制药股份有限公司 国药准字H20263158 2026/01/20 1ml:4mg(按C22H29FO5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
浙江仙琚制药股份有限公司浙江仙琚制药股份有限公司 国药准字H20263004 2026/01/05 1ml:4mg(按C22H29FO5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
新乡市常乐制药有限责任公司新乡市常乐制药有限责任公司 国药准字H20256197 2025/12/09 1ml : 4mg(按C22H29FO5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
新乡市常乐制药有限责任公司新乡市常乐制药有限责任公司 国药准字H20256196 2025/12/09 0.5ml : 2mg(按C22H29FO5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
漯河市汇创医药有限公司裕松源药业有限公司 国药准字H20255643 2025/09/30 1ml:4mg(按C22H29FO5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广州绿十字制药股份有限公司 国药准字H20255052 2025/07/29 1ml∶4mg(按C22H29FO5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
江苏神龙药业有限公司新乡市常乐制药有限责任公司 国药准字H20255017 2025/07/29 0.5ml:2mg(按C22H29FO5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
江苏神龙药业有限公司新乡市常乐制药有限责任公司 国药准字H20255016 2025/07/29 1ml:4mg(按C22H29FO5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
汇禹远和(海南)药业有限公司津药和平(天津)制药有限公司 国药准字H20254262 2025/05/27 1ml:4mg(按C22H29FO5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
辰欣药业股份有限公司辰欣药业股份有限公司 国药准字H20254363 2025/05/27 1ml:4mg(按C22H29FO5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
湖北民康药业集团有限公司津药和平(天津)制药有限公司 国药准字H20254024 2025/04/30 1ml∶4mg(按C22H29FO5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
裕松源药业有限公司裕松源药业有限公司 国药准字H20253583 2025/03/11 1ml∶4mg(按C22H29FO5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
陕西丽彩药业有限公司新乡市常乐制药有限责任公司 国药准字H20253417 2025/02/20 1ml:4mg(按C22H29FO5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
武汉天安医药科技有限公司津药和平(天津)制药有限公司 国药准字H20247307 2024/12/05 0.5ml:2mg(按C22H29FO5计) Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
武汉天安医药科技有限公司津药和平(天津)制药有限公司 国药准字H20058307 2024/12/05 1ml:4mg(按C22H29FO5计) Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
津药和平(天津)制药有限公司津药和平(天津)制药有限公司 国药准字H20249438 2024/11/22 1ml∶4mg(按C22H29FO5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H20244496 2024/07/30 1ml∶4mg(按C22H29FO5计) Not stated by sourceCDE
北京布霖生物科技有限公司华夏生生药业(北京)有限公司 国药准字H20244487 2024/07/30 1ml∶4mg(按C22H29FO5 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
成都倍特得诺药业有限公司成都倍特得诺药业有限公司 国药准字H20244470 2024/07/22 1ml:4mg(按C22H29FO5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
重庆华邦制药有限公司重庆华邦制药有限公司 国药准字H20243882 2024/06/04 1ml : 4mg(按C<sub>22</sub>H<sub>29</sub>FO<sub>5</sub>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
遂成药业股份有限公司遂成药业股份有限公司 国药准字H20064917 2023/08/29 1ml:4mg(按C22H29FO5计) Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
遂成药业股份有限公司遂成药业股份有限公司 国药准字H20064917 2023/08/29 0.5ml:2mg(按C22H29FO5计) Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
成都天台山制药股份有限公司成都天台山制药股份有限公司 国药准字H20265913 2026/09/08 1ml:4mg(按C22H29FO5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: 27 distinct approval numbers and 22 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
津药和平(天津)制药有限公司 国药准字H20249438 1ml∶4mg(按C22H29FO5计) Category B (乙) XH02ABB044B002010100874NHSA
重庆华邦制药有限公司 国药准字H20243882 1ml ꞉ 4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010101003NHSA
江苏神龙药业有限公司 国药准字H20255016 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010101478NHSA
武汉天安医药科技有限公司 国药准字H20058307 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010101866NHSA
四川美大康华康药业有限公司 国药准字H20264484 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010102087NHSA
裕松源药业有限公司 国药准字H20253583 1ml∶4mg(按C₂₂H₂₉FO₅ 计) Category B (乙) XH02ABB044B002010103163NHSA
遂成药业股份有限公司 国药准字H20064917 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010103204NHSA
新乡市常乐制药有限责任公司 国药准字H20256197 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010103216NHSA
辰欣药业股份有限公司 国药准字H20254363 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010104127NHSA
山东圣鲁制药有限公司 国药准字H20065249 1ml:2.63mg(相当于倍他米松2mg) Category B (乙) XH02ABB044B002010104207NHSA
浙江仙琚制药股份有限公司 国药准字H20263004 1ml:4mg(按C₂₂H₂₉FO₅ ‌计) Category B (乙) XH02ABB044B002010104735NHSA
云南龙海天然植物药业有限公司 国药准字H20263606 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010106286NHSA
华夏生生药业(北京)有限公司 国药准字H20244496 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010109910NHSA
成都倍特得诺药业有限公司 国药准字H20244470 1ml :4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010182338NHSA
陕西丽彩药业有限公司 国药准字H20253417 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010183540NHSA
汇禹远和(海南)药业有限公司 国药准字H20254262 1ml꞉4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010183867NHSA
北京六环药业有限公司 国药准字H20244487 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010183878NHSA
武汉天安医药科技有限公司 国药准字H20247307 0.5ml:2mg(按C22H29FO5计) Category B (乙) XH02ABB044B002010184397NHSA
安徽美来药业股份有限公司 国药准字H20265447 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010184482NHSA
成都瑞尔医药科技有限公司 国药准字H20255052 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010184534NHSA
湖北民康药业集团有限公司 国药准字H20254024 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010184564NHSA
重庆市义力医药科技有限公司 国药准字H20263689 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010184778NHSA
重庆华邦制药有限公司 国药准字H20243882 1ml ꞉ 4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010201003NHSA
武汉天安医药科技有限公司 国药准字H20058307 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010201866NHSA
裕松源药业有限公司 国药准字H20253583 1ml∶4mg(按C₂₂H₂₉FO₅ 计) Category B (乙) XH02ABB044B002010203163NHSA
遂成药业股份有限公司 国药准字H20064917 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010203204NHSA
辰欣药业股份有限公司 国药准字H20254363 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010204127NHSA
山东圣鲁制药有限公司 国药准字H20065249 1ml:2.63mg(相当于倍他米松2mg) Category B (乙) XH02ABB044B002010204207NHSA
浙江仙琚制药股份有限公司 国药准字H20263004 1ml:4mg(按C₂₂H₂₉FO₅ ‌计) Category B (乙) XH02ABB044B002010204735NHSA
成都倍特得诺药业有限公司 国药准字H20244470 1ml :4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010282338NHSA
陕西丽彩药业有限公司 国药准字H20253417 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010283540NHSA
武汉天安医药科技有限公司 国药准字H20247307 0.5ml:2mg(按C22H29FO5计) Category B (乙) XH02ABB044B002010284397NHSA
安徽美来药业股份有限公司 国药准字H20265447 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010284482NHSA
成都瑞尔医药科技有限公司 国药准字H20255052 1ml∶4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010284534NHSA
武汉天安医药科技有限公司 国药准字H20058307 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010301866NHSA
辰欣药业股份有限公司 国药准字H20254363 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010304127NHSA
辰欣药业股份有限公司 国药准字H20254363 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002010404127NHSA
江苏神龙药业有限公司 国药准字H20255017 0.5ml:2mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002020101478NHSA
漯河市汇创医药有限公司 国药准字H20255643 1ml:4mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002020103163NHSA
遂成药业股份有限公司 国药准字H20237102 0.5ml:2mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002020103204NHSA
新乡市常乐制药有限责任公司 国药准字H20256196 0.5ml:2mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002020103216NHSA
山东圣鲁制药有限公司 国药准字H20065250 1ml:5.26mg(相当于倍他米松4mg) Category B (乙) XH02ABB044B002020104207NHSA
遂成药业股份有限公司 国药准字H20237102 0.5ml:2mg(按C₂₂H₂₉FO₅计) Category B (乙) XH02ABB044B002020203204NHSA
山东圣鲁制药有限公司 国药准字H20065250 1ml:5.26mg(相当于倍他米松4mg) Category B (乙) XH02ABB044B002020204207NHSA

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: 5 filings and 5 distinct first applicants.

Generic 4 · Supplement 1

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
弘健制药(上海)有限公司;上海新华联制药有限公司 CYHS2601687 Generic2026/07/15Not stated by sourceCDE
江西科为制药有限公司;新乡市常乐制药有限责任公司 CYHS2600995 Generic2026/04/28Not stated by sourceCDE
河南润弘制药股份有限公司 CYHS2600316 Generic2026/01/30Not stated by sourceCDE
安徽均大高科医药科技有限公司;津药和平(天津)制药有限公司 CYHS2502807 Generic2025/08/04Not stated by sourceCDE
成都瑞尔医药科技有限公司;四川美大康华康药业有限公司;广州绿十字制药股份有限公司 CYHB2601954 Supplement2026/10/23Not stated by sourceCDE
New generic filings in 2026

Loaded records: 3 filings and 3 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
弘健制药(上海)有限公司;上海新华联制药有限公司 CYHS2601687 Generic2026/07/15Not stated by sourceCDE
江西科为制药有限公司;新乡市常乐制药有限责任公司 CYHS2600995 Generic2026/04/28Not stated by sourceCDE
河南润弘制药股份有限公司 CYHS2600316 Generic2026/01/30Not stated by sourceCDE
API registrations

Non-component matches: 7 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
倍他米松磷酸钠四川仁安药业有限责任公司Y20240001492AExact ingredient2026/11/04CDE
倍他米松磷酸钠河南利华制药有限公司Y20230000084AExact ingredient2025/10/27CDE
倍他米松磷酸钠CURIA SPAIN S.A.U.Y20230001012AExact ingredient2026/07/13CDE
倍他米松磷酸钠上海新华联制药有限公司Y20190009520AExact ingredient2025/02/20CDE
倍他米松磷酸钠浙江仙琚制药股份有限公司Y20190007551AExact ingredient2025/11/10CDE
倍他米松磷酸钠重庆胜凯制药有限公司Y20190006978AExact ingredient2025/08/09CDE
倍他米松磷酸钠津药药业股份有限公司Y20170002316AExact ingredient2026/01/24CDE

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. 2026/11/06No longer listed under review

    陕西顿斯制药有限公司

    CYHS2500399

    Fact date: 2026/11/06 · Site observation date: 2026/11/06

    Accepted: 2025/01/22

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

    View source ↗
  2. 2026/10/23Accepted

    成都瑞尔医药科技有限公司;四川美大康华康药业有限公司;广州绿十字制药股份有限公司

    CYHB2601954

    Fact date: 2026/10/23 · Site observation date: 2026/10/24

    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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