药格局YaoGeJu

Public drug landscapesDrug landscape

Phenylephrine Hydrochloride Injection(盐酸去氧肾上腺素注射液)

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: 22 holders; 1 in the quality-and-efficacy consistency-evaluation category, and 21 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
上海炫鑫医药科技有限公司山东方明药业集团股份有限公司 国药准字H20263044 2026/01/05 5ml:0.5mg 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
浙江博崤生物制药有限公司浙江博崤生物制药有限公司 国药准字H20256087 2025/11/25 1ml:10mg 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
北京海一药业有限公司广东星昊药业有限公司 国药准字H20255187 2025/08/26 5ml:0.5mg 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
成都苑东生物制药股份有限公司成都苑东生物制药股份有限公司 国药准字H20258164 2025/08/21 1ml:10mg 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
Mankind Pharma LimitedMankind Pharma Limited 国药准字HJ20250091 2025/07/29 1ml∶10mg 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
珠海前列药业有限公司湖南华纳大药厂股份有限公司 国药准字H20254858 2025/07/15 5ml:0.5mg 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
珠海前列药业有限公司湖南华纳大药厂股份有限公司 国药准字H20254857 2025/07/15 1ml:10mg 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
中润药业有限公司广东星昊药业有限公司 国药准字H20258118 2025/07/01 5ml:0.5mg 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
德全药品(江苏)股份有限公司德全药品(江苏)股份有限公司 国药准字H20254496 2025/06/10 1ml:10mg 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
安徽恒星制药有限公司安徽恒星制药有限公司 国药准字H20254431 2025/06/03 5ml:0.5mg 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
安徽长江药业有限公司安徽长江药业有限公司 国药准字H20254136 2025/05/13 1ml:10mg 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H20253246 2025/01/24 1ml:10mg 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H20253247 2025/01/24 10ml:100mg 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
海南倍特药业有限公司海南倍特药业有限公司 国药准字H20249840 2024/12/25 1ml∶10mg 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
海南倍特药业有限公司海南倍特药业有限公司 国药准字H20249841 2024/12/25 5ml∶0.5mg 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
中玉制药(海口)有限公司广东星昊药业有限公司 国药准字H20249726 2024/12/10 1ml:10mg 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
山东威智百科药业有限公司山东威智百科药业有限公司 国药准字H20249727 2024/12/10 5ml:0.5mg 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江苏大红鹰恒顺药业有限公司 国药准字H20249211 2024/10/29 1ml:10mg 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H20249214 2024/10/29 1ml:10mg 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
南京海融医药科技股份有限公司南京海融制药有限公司 国药准字H20243723 2024/05/15 5ml:0.5mg 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
南京海融医药科技股份有限公司南京海融制药有限公司 国药准字H20243722 2024/05/15 1ml:10mg 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四川美大康佳乐药业有限公司 国药准字H20243673 2024/05/08 1ml:10mg 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四川美大康佳乐药业有限公司 国药准字H20243674 2024/05/08 5ml:0.5mg 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
舒美奇成都生物科技有限公司四川美大康佳乐药业有限公司 国药准字H20243558 2024/04/24 5ml:0.5mg 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
舒美奇成都生物科技有限公司四川美大康佳乐药业有限公司 国药准字H20243559 2024/04/24 1ml:10mg 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
上海禾丰制药有限公司上海禾丰制药有限公司 国药准字H31021175 2023/08/10 1ml:10mg Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) CDE
中润药业有限公司广东星昊药业有限公司 国药准字H20233385 2023/03/24 1ml:10mg 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
合肥亿帆生物制药有限公司合肥亿帆生物制药有限公司 国药准字H20233387 2023/03/24 1ml:10mg 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
成都苑东生物制药股份有限公司成都苑东生物制药股份有限公司 国药准字H20223286 2022/05/10 5ml:0.5mg 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云南龙海天然植物药业有限公司 国药准字H20255469 2025/09/09 5ml︰0.5mg 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: 29 distinct approval numbers and 21 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
上海禾丰制药有限公司 国药准字H31021175 1ml:10mg Category B (乙) XC01CAQ130B002010100673NHSA
德全药品(江苏)股份有限公司 国药准字H20254496 1ml:10mg Category B (乙) XC01CAQ130B002010101751NHSA
成都苑东生物制药股份有限公司 国药准字H20223286 5ml:0.5mg Category B (乙) XC01CAQ130B002010102181NHSA
中润药业有限公司 国药准字H20258118 5ml:0.5mg Category B (乙) XC01CAQ130B002010102699NHSA
石家庄四药有限公司 国药准字H20249214 1ml:10mg Category B (乙) XC01CAQ130B002010102763NHSA
安徽长江药业有限公司 国药准字H20254136 1ml:10mg Category B (乙) XC01CAQ130B002010104451NHSA
海南倍特药业有限公司 国药准字H20249841 5ml∶0.5mg Category B (乙) XC01CAQ130B002010105791NHSA
海南普利制药股份有限公司 国药准字H20253246 1ml:10mg Category B (乙) XC01CAQ130B002010105801NHSA
云南龙海天然植物药业有限公司 国药准字H20255469 5ml:0.5mg Category B (乙) XC01CAQ130B002010106286NHSA
安徽恒星制药有限公司 国药准字H20254431 5ml:0.5mg Category B (乙) XC01CAQ130B002010107478NHSA
合肥亿帆生物制药有限公司 国药准字H20233387 1ml:10mg Category B (乙) XC01CAQ130B002010182719NHSA
南京恒道医药科技股份有限公司 国药准字H20249211 1ml:10mg Category B (乙) XC01CAQ130B002010183035NHSA
山东威智百科药业有限公司 国药准字H20249727 5ml:0.5mg Category B (乙) XC01CAQ130B002010183124NHSA
中玉制药(海口)有限公司 国药准字H20249726 1ml:10mg Category B (乙) XC01CAQ130B002010183237NHSA
中润药业有限公司 国药准字H20233385 1ml:10mg Category B (乙) XC01CAQ130B002010183256NHSA
舒美奇成都生物科技有限公司 国药准字H20243558 5ml:0.5mg Category B (乙) XC01CAQ130B002010183337NHSA
远大医药(中国)有限公司 国药准字H20253388 1ml:10mg Category B (乙) XC01CAQ130B002010183383NHSA
南京海融制药有限公司 国药准字H20243722 1ml∶10mg Category B (乙) XC01CAQ130B002010183564NHSA
成都瑞尔医药科技有限公司 国药准字H20243673 1ml:10mg Category B (乙) XC01CAQ130B002010184534NHSA
北京海一药业有限公司 国药准字H20255187 5ml:0.5mg Category B (乙) XC01CAQ130B002010185058NHSA
珠海前列药业有限公司 国药准字H20254857 1ml:10mg Category B (乙) XC01CAQ130B002010185087NHSA
Mankind Pharma Limited 国药准字HJ20250091 1ml:10mg Category B (乙) XC01CAQ130B002010185454NHSA
上海禾丰制药有限公司 国药准字H31021175 1ml:10mg Category B (乙) XC01CAQ130B002010200673NHSA
德全药品(江苏)股份有限公司 国药准字H20254496 1ml:10mg Category B (乙) XC01CAQ130B002010201751NHSA
成都苑东生物制药股份有限公司 国药准字H20223286 5ml:0.5mg Category B (乙) XC01CAQ130B002010202181NHSA
石家庄四药有限公司 国药准字H20249214 1ml:10mg Category B (乙) XC01CAQ130B002010202763NHSA
安徽长江药业有限公司 国药准字H20254136 1ml:10mg Category B (乙) XC01CAQ130B002010204451NHSA
海南倍特药业有限公司 国药准字H20249841 5ml∶0.5mg Category B (乙) XC01CAQ130B002010205791NHSA
海南普利制药股份有限公司 国药准字H20253246 1ml:10mg Category B (乙) XC01CAQ130B002010205801NHSA
云南龙海天然植物药业有限公司 国药准字H20255469 5ml:0.5mg Category B (乙) XC01CAQ130B002010206286NHSA
安徽恒星制药有限公司 国药准字H20254431 5ml:0.5mg Category B (乙) XC01CAQ130B002010207478NHSA
合肥亿帆生物制药有限公司 国药准字H20233387 1ml:10mg Category B (乙) XC01CAQ130B002010282719NHSA
南京恒道医药科技股份有限公司 国药准字H20249211 1ml:10mg Category B (乙) XC01CAQ130B002010283035NHSA
中润药业有限公司 国药准字H20233385 1ml:10mg Category B (乙) XC01CAQ130B002010283256NHSA
舒美奇成都生物科技有限公司 国药准字H20243558 5ml:0.5mg Category B (乙) XC01CAQ130B002010283337NHSA
南京海融制药有限公司 国药准字H20243722 1ml∶10mg Category B (乙) XC01CAQ130B002010283564NHSA
成都瑞尔医药科技有限公司 国药准字H20243673 1ml:10mg Category B (乙) XC01CAQ130B002010284534NHSA
Mankind Pharma Limited 国药准字HJ20250091 1ml:10mg Category B (乙) XC01CAQ130B002010285454NHSA
上海禾丰制药有限公司 国药准字H31021175 1ml:10mg Category B (乙) XC01CAQ130B002010300673NHSA
海南普利制药股份有限公司 国药准字H20253246 1ml:10mg Category B (乙) XC01CAQ130B002010305801NHSA
中润药业有限公司 国药准字H20233385 1ml:10mg Category B (乙) XC01CAQ130B002010383256NHSA
南京海融制药有限公司 国药准字H20243722 1ml∶10mg Category B (乙) XC01CAQ130B002010383564NHSA
海南普利制药股份有限公司 国药准字H20253246 1ml:10mg Category B (乙) XC01CAQ130B002010405801NHSA
成都苑东生物制药股份有限公司 国药准字H20258164 1ml:10mg Category B (乙) XC01CAQ130B002020102181NHSA
海南倍特药业有限公司 国药准字H20249840 1ml∶10mg Category B (乙) XC01CAQ130B002020105791NHSA
海南普利制药股份有限公司 国药准字H20253247 10ml:100mg Category B (乙) XC01CAQ130B002020105801NHSA
舒美奇成都生物科技有限公司 国药准字H20243559 1ml:10mg Category B (乙) XC01CAQ130B002020183337NHSA
南京海融制药有限公司 国药准字H20243723 5ml:0.5mg Category B (乙) XC01CAQ130B002020183564NHSA
成都瑞尔医药科技有限公司 国药准字H20243674 5ml:0.5mg Category B (乙) XC01CAQ130B002020184534NHSA
珠海前列药业有限公司 国药准字H20254858 5ml:0.5mg Category B (乙) XC01CAQ130B002020185087NHSA
成都苑东生物制药股份有限公司 国药准字H20258164 1ml:10mg Category B (乙) XC01CAQ130B002020202181NHSA
舒美奇成都生物科技有限公司 国药准字H20243559 1ml:10mg Category B (乙) XC01CAQ130B002020283337NHSA
南京海融制药有限公司 国药准字H20243723 5ml:0.5mg Category B (乙) XC01CAQ130B002020283564NHSA
成都瑞尔医药科技有限公司 国药准字H20243674 5ml:0.5mg Category B (乙) XC01CAQ130B002020284534NHSA
成都苑东生物制药股份有限公司 国药准字H20258164 1ml:10mg Category B (乙) XC01CAQ130B002020302181NHSA
南京海融制药有限公司 国药准字H20243723 5ml:0.5mg Category B (乙) XC01CAQ130B002020383564NHSA
海南倍特药业有限公司 国药准字H20249840 1ml∶10mg Category B (乙) XC01CAQ130B002030105791NHSA

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 3 distinct first applicants.

Generic 5

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
江苏福邦药业有限公司 CYHS2602101 Generic2026/08/24Not stated by sourceCDE
江苏福邦药业有限公司 CYHS2602100 Generic2026/08/24Not stated by sourceCDE
广州市联瑞制药有限公司 CYHS2600381 Generic2026/02/05Not stated by sourceCDE
绪必迪药业(沧州)有限公司;河北凯威制药有限责任公司 CYHS2600259 Generic2026/01/23Not stated by sourceCDE
绪必迪药业(沧州)有限公司;河北凯威制药有限责任公司 CYHS2600258 Generic2026/01/23Not stated by sourceCDE
New generic filings in 2026

Loaded records: 5 filings and 3 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
江苏福邦药业有限公司 CYHS2602101 Generic2026/08/24Not stated by sourceCDE
江苏福邦药业有限公司 CYHS2602100 Generic2026/08/24Not stated by sourceCDE
广州市联瑞制药有限公司 CYHS2600381 Generic2026/02/05Not stated by sourceCDE
绪必迪药业(沧州)有限公司;河北凯威制药有限责任公司 CYHS2600259 Generic2026/01/23Not stated by sourceCDE
绪必迪药业(沧州)有限公司;河北凯威制药有限责任公司 CYHS2600258 Generic2026/01/23Not stated by sourceCDE
API registrations

Non-component matches: 10 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
盐酸去氧肾上腺素湖南华纳大药厂手性药物有限公司Y20260000025IExact ingredient2026/02/12CDE
盐酸去氧肾上腺素绪必迪药业(沧州)有限公司Y20250000477IExact ingredient2025/05/22CDE
盐酸去氧肾上腺素武汉武药制药有限公司Y20240000593AExact ingredient2026/01/14CDE
盐酸去氧肾上腺素湖北美林药业有限公司Y20240000416AExact ingredient2025/12/17CDE
盐酸去氧肾上腺素浙江博崤生物制药有限公司Y20240000091AExact ingredient2025/11/22CDE
盐酸去氧肾上腺素安徽恒星制药有限公司Y20230000387AExact ingredient2025/03/19CDE
盐酸去氧肾上腺素河北广祥制药有限公司Y20220001108AExact ingredient2025/07/16CDE
盐酸去氧肾上腺素Malladi Drugs & Pharmaceuticals LimitedY20210000760AExact ingredient2025/01/15CDE
盐酸去氧肾上腺素深圳沃兰德药业有限公司Y20190009335AExact ingredient2026/03/26CDE
盐酸去氧肾上腺素赤峰艾克制药科技股份有限公司Y20190004873AExact ingredient2024/10/10CDE
盐酸去氧肾上腺素浙江海翔川南药业有限公司Y20170001393AExact ingredient2024/04/10CDE
盐酸去氧肾上腺素DIVI'S LABORATORIES LTDY20170000948AExact ingredient2026/09/12CDE

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. 2026/08/24Accepted

    江苏福邦药业有限公司

    CYHS2602101

    Fact date: 2026/08/24 · Site observation date: 2026/10/21

    View source ↗
  2. 2026/08/24Accepted

    江苏福邦药业有限公司

    CYHS2602100

    Fact date: 2026/08/24 · Site observation date: 2026/10/21

    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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