药格局YaoGeJu

Public drug landscapesDrug landscape

帕拉米韦氯化钠注射液

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

Last 90 days: Marketing application approved: 1 applicationAccepted: 2 applications

Current coverage may be incomplete

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: 8 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 8 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
博智安健(河北)药业有限公司山东华鲁制药有限公司 国药准字H20265274 2026/07/21 100ml︰帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
广东大翔制药有限公司广东大翔制药有限公司 国药准字H20264777 2026/06/10 100ml:帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
江苏长江药业有限公司江苏长江药业有限公司 国药准字H20264458 2026/05/19 100ml:帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
江苏长江药业有限公司江苏长江药业有限公司 国药准字H20264459 2026/05/19 100ml:帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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
石家庄四药有限公司石家庄四药有限公司 国药准字H20264443 2026/05/19 100ml︰帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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
石家庄四药有限公司石家庄四药有限公司 国药准字H20264442 2026/05/19 100ml︰帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
湖南九维生物医药有限公司湖南金健药业有限责任公司 国药准字H20264215 2026/04/29 100ml︰帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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
湖南九维生物医药有限公司湖南金健药业有限责任公司 国药准字H20264216 2026/04/29 100ml︰帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
南京恒道医药科技股份有限公司武汉福星生物药业有限公司 国药准字H20263763 2026/03/31 100ml︰帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
仁合益康集团有限公司河北仁合益康药业有限公司 国药准字H20255760 2025/10/21 100ml 帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
仁合益康集团有限公司河北仁合益康药业有限公司 国药准字H20255761 2025/10/21 100ml 帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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H20255050 2025/07/29 100ml︰帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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H20255049 2025/07/29 100ml:帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g 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
广东大翔制药有限公司广东大翔制药有限公司 国药准字H20264778 2026/06/10 100ml:帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g 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: 16 distinct approval numbers and 9 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
广州南新制药有限公司 国药准字H20170004 100ml:帕拉米韦(按C15H28N4O4计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010100407NHSA
江苏长江药业有限公司 国药准字H20264458 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010101426NHSA
石家庄四药有限公司 国药准字H20264443 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002010102763NHSA
山东齐都药业有限公司 国药准字H20255049 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010104145NHSA
湖南九维生物医药有限公司 国药准字H20264215 100ml 帕拉米韦(按C₁₅H₂₈N₄O₄ 计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002010104936NHSA
广东大翔制药有限公司 国药准字H20264778 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002010109938NHSA
仁合益康集团有限公司 国药准字H20255760 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010183033NHSA
南京恒道医药科技股份有限公司 国药准字H20263763 100ml : 帕拉米韦(按C₁₅H₂₈N₄O₄ 计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010183035NHSA
博智安健(河北)药业有限公司 国药准字H20265274 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄ 计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010185749NHSA
仁合益康集团有限公司 国药准字H20255760 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002010283033NHSA
广州南新制药有限公司 国药准字H20130029 100ml:帕拉米韦(按C15H28N4O4计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002020100407NHSA
江苏长江药业有限公司 国药准字H20264459 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002020101426NHSA
石家庄四药有限公司 国药准字H20264442 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002020102763NHSA
山东齐都药业有限公司 国药准字H20255050 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002020104145NHSA
湖南九维生物医药有限公司 国药准字H20264216 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002020104936NHSA
广东大翔制药有限公司 国药准字H20264777 100ml:帕拉米韦(按C₁₅H₂₈N₄O₄计)0.15g与氯化钠0.9g Category B (乙) XJ05AHP119B002020109938NHSA
仁合益康集团有限公司 国药准字H20255761 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002020183033NHSA
仁合益康集团有限公司 国药准字H20255761 100ml︰帕拉米韦(按C₁₅H₂₈N₄O₄计)0.3g与氯化钠0.9g Category B (乙) XJ05AHP119B002020283033NHSA

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: 17 filings and 9 distinct first applicants.

Generic 17

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
苏州第壹制药有限公司;浙江国镜药业有限公司 CYHS2600435 Generic2026/02/10Not stated by sourceCDE
苏州第壹制药有限公司;浙江国镜药业有限公司 CYHS2600434 Generic2026/02/10Not stated by sourceCDE
江苏亚尧生物科技有限公司;安徽丰原药业股份有限公司 CYHS2502364 Generic2025/07/04Not stated by sourceCDE
江苏亚尧生物科技有限公司;安徽丰原药业股份有限公司 CYHS2502363 Generic2025/07/04Not stated by sourceCDE
信合援生制药股份有限公司 CYHS2601388 Generic2026/06/11Not stated by sourceCDE
信合援生制药股份有限公司 CYHS2601387 Generic2026/06/11Not stated by sourceCDE
四川健林药业有限责任公司;扬子江药业集团四川海蓉药业有限公司 CYHS2600368 Generic2026/02/04Not stated by sourceCDE
辰欣药业股份有限公司 CYHS2504220 Generic2025/12/09Not stated by sourceCDE
辰欣药业股份有限公司 CYHS2504219 Generic2025/12/09Not stated by sourceCDE
浙江康吉尔药业有限公司 CYHS2503382 Generic2025/09/12Not stated by sourceCDE
浙江康吉尔药业有限公司 CYHS2503381 Generic2025/09/12Not stated by sourceCDE
珠海同源药业有限公司 CYHS2503167 Generic2025/08/29Not stated by sourceCDE
珠海同源药业有限公司 CYHS2503166 Generic2025/08/29Not stated by sourceCDE
哈尔滨三联药业股份有限公司 CYHS2503015 Generic2025/08/16Not stated by sourceCDE
哈尔滨三联药业股份有限公司 CYHS2503014 Generic2025/08/16Not stated by sourceCDE
河北天成药业股份有限公司 CYHS2602675 Generic2026/11/02Not stated by sourceCDE
河北天成药业股份有限公司 CYHS2602674 Generic2026/11/02Not stated by sourceCDE
New generic filings in 2026

Loaded records: 7 filings and 4 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
苏州第壹制药有限公司;浙江国镜药业有限公司 CYHS2600435 Generic2026/02/10Not stated by sourceCDE
苏州第壹制药有限公司;浙江国镜药业有限公司 CYHS2600434 Generic2026/02/10Not stated by sourceCDE
信合援生制药股份有限公司 CYHS2601388 Generic2026/06/11Not stated by sourceCDE
信合援生制药股份有限公司 CYHS2601387 Generic2026/06/11Not stated by sourceCDE
四川健林药业有限责任公司;扬子江药业集团四川海蓉药业有限公司 CYHS2600368 Generic2026/02/04Not stated by sourceCDE
河北天成药业股份有限公司 CYHS2602675 Generic2026/11/02Not stated by sourceCDE
河北天成药业股份有限公司 CYHS2602674 Generic2026/11/02Not 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. 2026/11/03Marketing application approved

    山西诺成制药有限公司

    CYHS2501707 · 国药准字H20266470

    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 72 ↗
  2. 2026/11/02Accepted

    河北天成药业股份有限公司

    CYHS2602675

    Fact date: 2026/11/02 · Site observation date: 2026/11/03

    View source ↗
  3. 2026/11/02Accepted

    河北天成药业股份有限公司

    CYHS2602674

    Fact date: 2026/11/02 · Site observation date: 2026/11/03

    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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