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Menatetrenone Soft Capsules

As of 13 November 2026, for Menatetrenone Soft Capsules, 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
Kunming Bang Yu Pharmaceutical Co., Ltd. romanizedKunming Bang Yu Pharmaceutical Co., Ltd. romanized国药准字H202658642026/09/0215mgGeneric approved under the new chemical-drug registration classificationCDE
Henan Tai Feng Bio Technology Co., Ltd. romanizedHenan Tai Feng Bio Technology Co., Ltd. romanized国药准字H202532822025/01/2415mgGeneric 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: 4 distinct approval numbers and 2 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Eisai Co.,Ltd.国药准字J2015011315mgNot stated by sourceXB02BAS220E002010101693NHSA
Henan Tai Feng Bio Technology Co., Ltd. romanized国药准字H2025328215mgNot stated by sourceXB02BAS220E002010103013NHSA
Eisai Co.,Ltd.H2015011515mgNot stated by sourceXB02BAS220E002010179086NHSA
Henan Tai Feng Bio Technology Co., Ltd. romanized国药准字H2025328215mgNot stated by sourceXB02BAS220E002010203013NHSA
Eisai Co.,Ltd.H2015011515mgNot stated by sourceXB02BAS220E002010279086NHSA
Eisai Co., Ltd.国药准字HJ2015011415mgNot stated by sourceXB02BAS220E002010479086NHSA

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
Nanjing Hai Rong Pharmaceutical Co., Ltd. romanizedCYHS2503494Generic2025/09/23Not stated by sourceCDE
Nanjing Hai Jing Pharma Co., Ltd. romanizedCYHS2602550Generic2026/10/16Not stated by sourceCDE
Hua Xia Guo Yao (He Ze) Pharmaceutical Co., Ltd. romanizedCYHS2601551Generic2026/07/01Not stated by sourceCDE
Zhejiang He Li Xin Jian Pharma Co., Ltd. romanized; Zhejiang Qian Yuan Hai Li Sheng Pharmaceutical Co., Ltd. romanizedCYHS2502377Generic2025/07/05Not stated by sourceCDE
New generic filings in 2026

Loaded records: 3 filings and 2 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Nanjing Hai Jing Pharma Co., Ltd. romanizedCYHS2602550Generic2026/10/16Not stated by sourceCDE
Hua Xia Guo Yao (He Ze) Pharmaceutical Co., Ltd. romanizedCYHS2601551Generic2026/07/01Not stated by sourceCDE
Hua Xia Guo Yao (He Ze) Pharmaceutical Co., Ltd. romanizedCYHS2601032Generic2026/05/07Not stated by sourceCDE
API registrations

Non-component matches: 6 companies with A status and 4 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
四烯甲萘醌 · No verified English nameShenyang San Jiu Pharma Co., Ltd. romanizedY20260000787IExact ingredient2026/10/08CDE
四烯甲萘醌 · No verified English nameNanjing Hai Jing Pharma Co., Ltd. romanizedY20260000633IExact ingredient2026/08/05CDE
四烯甲萘醌 · No verified English nameXian De Li Bio Chemical Co., Ltd. romanizedY20260000140IExact ingredient2026/03/12CDE
四烯甲萘醌 · No verified English nameWei Nan Rui Lian Pharmaceutical Co., Ltd. romanizedY20250000519AExact ingredient2026/11/10CDE
四烯甲萘醌 · No verified English nameHunan Xian Shi Pharmaceutical Co., Ltd. romanizedY20250000438IExact ingredient2025/05/13CDE
四烯甲萘醌 · No verified English nameZhejiang Hua Na Pharma Co., Ltd. romanizedY20250000270AExact ingredient2026/10/16CDE
四烯甲萘醌 · No verified English nameWei Zhi Pharmaceuticals Co., Ltd. romanizedY20240001239AExact ingredient2026/09/21CDE
四烯甲萘醌 · No verified English nameShandong Xin Shi Dai Pharma Co., Ltd. romanizedY20240000634AExact ingredient2026/02/02CDE
四烯甲萘醌 · No verified English nameNAKODA CHEMICALS LIMITEDY20240000172AExact ingredient2025/11/11CDE
四烯甲萘醌 · No verified English nameZhengzhou Tai Feng Pharmaceutical Co., Ltd. romanizedY20230000501AExact ingredient2024/10/15CDE

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. 2026/10/16Accepted

    Nanjing Hai Jing Pharma Co., Ltd. romanized

    CYHS2602550

    Fact date: 2026/10/16 · Site observation date: 2026/10/21

    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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