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Estradiol Tablets

As of 13 November 2026, for Estradiol Tablets, 3 applications are listed as under review at China's CDE; 3 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 1 holder.

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
2026/11/13 06:42
Matching scope
Same generic name; dosage forms and combinations kept separate

US Orange Book listing

The brand names come from the US FDA Orange Book and describe US listing records for this active ingredient. They do not indicate that products under these brand names are approved or sold in China, or that Chinese applicants are affiliated with US holders.

Orange Book source export date: 2026/11/06. Version: 2026-11-06.

Showing 5 of 16 distinct brand names.

A brand with different source forms or statuses can appear on multiple rows and in both groups. Distinct brand names are counted once globally, with a limit of five.

Verified official English dosage form: Tablets. Listings are grouped by the source dosage form and route; records without a clear correspondence are listed in the other group. Grouping does not establish product equivalence.

Same dosage form

No listings in this group among the displayed brand names.

Other dosage forms of the same ingredient

Brand nameApplicant (source text)Application numberDosage form (source text)Route (source text)Marketing status (source text)Approval date
CLIMARA BAYER HEALTHCARE PHARMACEUTICALS INC NDA 020375 · Product no. 001, 002 FILM, EXTENDED RELEASE TRANSDERMAL HUMAN PRESCRIPTION DRUG 1994/12/22
ESTRING PFIZER INC NDA 020472 · Product no. 001 INSERT, EXTENDED RELEASE VAGINAL HUMAN PRESCRIPTION DRUG 1996/04/26
CLIMARA BAYER HEALTHCARE PHARMACEUTICALS INC NDA 020375 · Product no. 003 FILM, EXTENDED RELEASE TRANSDERMAL HUMAN PRESCRIPTION DRUG 1998/03/23
VIVELLE-DOT SANDOZ INC NDA 020538 · Product no. 005, 006, 007, 008 SYSTEM TRANSDERMAL HUMAN PRESCRIPTION DRUG 1999/01/08
CLIMARA BAYER HEALTHCARE PHARMACEUTICALS INC NDA 020375 · Product no. 004 FILM, EXTENDED RELEASE TRANSDERMAL HUMAN PRESCRIPTION DRUG 1999/03/05
VIVELLE-DOT SANDOZ INC NDA 020538 · Product no. 009 SYSTEM TRANSDERMAL HUMAN PRESCRIPTION DRUG 2002/05/03
CLIMARA BAYER HEALTHCARE PHARMACEUTICALS INC NDA 020375 · Product no. 005, 006 FILM, EXTENDED RELEASE TRANSDERMAL HUMAN PRESCRIPTION DRUG 2003/05/27
ESTROGEL ASCEND THERAPEUTICS US LLC NDA 021166 · Product no. 002 GEL, METERED TRANSDERMAL HUMAN PRESCRIPTION DRUG 2004/02/09
MENOSTAR BAYER HEALTHCARE PHARMACEUTICALS INC NDA 021674 · Product no. 001 SYSTEM TRANSDERMAL HUMAN PRESCRIPTION DRUG 2004/06/08
ESTROGEL ASCEND THERAPEUTICS US LLC NDA 021166 · Product no. 001 GEL TOPICAL DISCONTINUED 2004/02/09

Same-form/route listings come first, followed by other forms/routes. Within each group, source prescription/OTC listings precede discontinued listings; unknown statuses are last. Each status bucket is ordered by earliest approval date, ascending: pre-1982 records first, missing dates last; ties by brand name, application number and product number. The first five distinct brands in this order are selected globally. All retained source facts for those brands are shown in their own groups; a brand spanning both groups counts once.

Ingredient cross-list details ↗

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: 1 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 1 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanizedZhejiang Xian Ju Pharmaceutical Co., Ltd. romanized国药准字H202554912025/09/161mgGeneric 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: 1 distinct approval numbers and 1 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanized国药准字H202554911mgNot stated by sourceXG03CAC050A001010104735NHSA

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: 3 filings and 3 distinct first applicants.

Generic 3

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Yang Zhou Ao Rui Te Pharma Co., Ltd. romanizedCYHS2601908Generic2026/08/05Not stated by sourceCDE
Beijing Jin Cheng Tai Er Pharmaceutical Co., Ltd. romanizedCYHS2602565Generic2026/10/19Not stated by sourceCDE
Hangzhou Bei Te Biopharmaceuticals Co., Ltd. romanizedCYHS2602649Generic2026/10/29Not 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
Yang Zhou Ao Rui Te Pharma Co., Ltd. romanizedCYHS2601908Generic2026/08/05Not stated by sourceCDE
Beijing Jin Cheng Tai Er Pharmaceutical Co., Ltd. romanizedCYHS2602565Generic2026/10/19Not stated by sourceCDE
Hangzhou Bei Te Biopharmaceuticals Co., Ltd. romanizedCYHS2602649Generic2026/10/29Not stated by sourceCDE
API registrations

Non-component matches: 7 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
雌二醇 · No verified English nameYang Zhou Ao Rui Te Pharma Co., Ltd. romanizedY20260000482IExact ingredient2026/06/23CDE
雌二醇 · No verified English nameSichuan Ren An Pharma Co., Ltd. romanizedY20250001438IExact ingredient2026/02/27CDE
雌二醇 · No verified English nameShaanxi Han Jiang Pharma Group Co., Ltd. romanizedY20250000102AExact ingredient2026/10/10CDE
雌二醇 · No verified English nameHunan Ke Yi Xin Biopharmaceuticals Co., Ltd. romanizedY20240001336AExact ingredient2026/04/21CDE
雌二醇 · No verified English nameAspen Oss B.V.Y20220000142AExact ingredient2024/04/16CDE
雌二醇 · No verified English nameBeijing Shi Ke Yi Feng Bio Technology Development Co., Ltd. romanizedY20190008488AExact ingredient—CDE
雌二醇 · No verified English nameZhejiang Xian Ju Pharmaceutical Co., Ltd. romanizedY20190007536AExact ingredient2024/01/27CDE
苯甲酸雌二醇 · No verified English nameZhejiang Xian Ju Pharmaceutical Co., Ltd. romanizedY20190007533ASalt-normalized ingredient2024/01/17CDE
雌二醇 · No verified English nameQin Huang Dao Zi Zhu Pharma Co., Ltd. romanizedY20190006443AExact ingredient2026/09/01CDE
雌二醇 · No verified English nameHubei Ge Dian Ren Fu Pharma Co., Ltd. romanizedY20170000527AExact ingredient2025/12/03CDE

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. 2026/10/29Accepted

    Hangzhou Bei Te Biopharmaceuticals Co., Ltd. romanized

    CYHS2602649

    Fact date: 2026/10/29 · Site observation date: 2026/10/30

    View source ↗
  2. 2026/10/19Accepted

    Beijing Jin Cheng Tai Er Pharmaceutical Co., Ltd. romanized

    CYHS2602565

    Fact date: 2026/10/19 · 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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