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Vincriscristine Sulfate Injection

As of 13 November 2026, for Vincriscristine Sulfate Injection, 4 applications are listed as under review at China's CDE; 2 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 2 holders.

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

Last 90 days: Accepted: 1 application

Current coverage may be incomplete

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Complete CDE snapshot
2026/11/13 06:42
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.

Legal reference identifiers are retained verbatim. Company labels use official English entries where available, or a visibly marked fixed romanization. Unverified drug names retain the Chinese source name with a No verified English name marker. Other Chinese free text is not displayed; use the source links or source-name columns in CSV exports.

Chemical-drug catalogue

Loaded records: 2 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 2 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Hainan Mei Kang Da Pharma Co., Ltd. romanizedHefei Yi Fan Biopharmaceutical Co., Ltd. romanized国药准字H202436892024/05/151ml:1mgGeneric approved under the new chemical-drug registration classificationCDE
Hefei Yi Fan Biopharmaceutical Co., Ltd. romanizedHefei Yi Fan Biopharmaceutical Co., Ltd. romanized国药准字H202332252023/02/281ml∶1mgGeneric approved under the new chemical-drug registration classificationCDE

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: 2 distinct approval numbers and 2 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Hefei Yi Fan Biopharmaceutical Co., Ltd. romanized国药准字H202332251ml∶1mgCategory AXL01CAC022B002010182719NHSA
Hainan Mei Kang Da Pharma Co., Ltd. romanized国药准字H202436891ml:1mgCategory AXL01CAC022B002010183920NHSA

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: 4 filings and 4 distinct first applicants.

Generic 4

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Shenzhen Wan Le Pharma Co., Ltd. romanizedCYHS2602076Generic2026/08/20Not stated by sourceCDE
Ren He Xi De Long Pharma Co., Ltd. romanizedCYHS2600496Generic2026/02/25Not stated by sourceCDE
Ji Si Mei (Wuhan) Pharmaceutical Co., Ltd. romanizedCYHS2503117Generic2025/08/26Not stated by sourceCDE
Hainan Brilliant Pharmaceutical Co., Ltd.CYHS2502160Generic2025/06/17Not 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
Shenzhen Wan Le Pharma Co., Ltd. romanizedCYHS2602076Generic2026/08/20Not stated by sourceCDE
Ren He Xi De Long Pharma Co., Ltd. romanizedCYHS2600496Generic2026/02/25Not stated by sourceCDE
API registrations

Non-component matches: 7 companies with A status and 1 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
硫酸长春新碱 · No verified English nameSichuan Ren An Pharma Co., Ltd. romanizedY20240001531AExact ingredient2026/06/02CDE
硫酸长春新碱 · No verified English nameHubei Hong Zhong Pharma Co., Ltd. romanizedY20240001296AExact ingredient2026/06/30CDE
硫酸长春新碱 · No verified English nameSu Zhou Yi Fan Pharma Co., Ltd. romanizedY20240001158AExact ingredient2026/03/02CDE
硫酸长春新碱 · No verified English nameGuangzhou Bai Yun Shan Han Fang Xian Dai Pharma Co., Ltd. romanizedY20190009906AExact ingredient2026/05/20CDE
硫酸长春新碱 · No verified English nameHainan Changchun Hua Pharma Co., Ltd. romanizedY20190009843AExact ingredient2025/01/25CDE
硫酸长春新碱 · No verified English nameJiangsu Sheng Qin Fen Pharma Co., Ltd. romanizedY20190003072AExact ingredient—CDE
硫酸长春新碱 · No verified English nameZhejiang Hai Zheng Pharma Co., Ltd. romanizedY20190001747AExact ingredient2024/08/27CDE
硫酸长春新碱 · No verified English nameHainan Changchun Hua Pharma Co., Ltd. romanizedY20190000094IExact ingredient2019/03/01CDE

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: 2026/11/13 06:39. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.

This source was last successfully updated at 2026/11/12 18:32; current coverage may be incomplete.

  1. 2026/08/20Accepted

    Shenzhen Wan Le Pharma Co., Ltd. romanized

    CYHS2602076

    Fact date: 2026/08/20 · Site observation date: 2026/10/22

    View source ↗

How current is each source?

CDE acceptances and review
Last successful update: 2026/11/13 06:42
Chemical-drug catalogue
Last successful update: 2026/11/13 06:39

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: 2026/11/13 06:41
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: 2026/11/12 18:32 · Current coverage may be incomplete

First index-page publication dates: 2026-10-29 to 2026-11-13; 2 pages pending. Covers loaded notices only, not a complete historical approval database.

Drug Clinical Trial Registry and Information Disclosure Platform
Last successful update: 2026/11/13 08:09 · 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: 7/30; discovered pending details: 13. 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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