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Dolutegravir Sodium Tablets

As of 13 November 2026, for Dolutegravir Sodium Tablets, 3 applications are listed as under review at China's CDE; 2 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 6 holders.

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

Listed in the US FDA Orange Book as TIVICAY (NDA 204790, VIIV HEALTHCARE CO).

Last 90 days: Marketing application approved: 1 applicationAccepted: 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

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 2 of 2 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

Brand nameApplicant (source text)Application numberDosage form (source text)Route (source text)Marketing status (source text)Approval date
TIVICAY VIIV HEALTHCARE CO NDA 204790 · Product no. 001 TABLET ORAL HUMAN PRESCRIPTION DRUG 2013/08/12
TIVICAY VIIV HEALTHCARE CO NDA 204790 · Product no. 002, 003 TABLET ORAL DISCONTINUED 2016/06/09

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
TIVICAY PD VIIV HEALTHCARE CO NDA 213983 · Product no. 001 TABLET, FOR SUSPENSION ORAL HUMAN PRESCRIPTION DRUG 2020/06/12

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: 6 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 6 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Ao Rui Te Pharma Co., Ltd. romanizedJiangsu He Chen Pharma Co., Ltd. romanized国药准字H202642252026/05/07See sourceGeneric approved under the new chemical-drug registration classificationCDE
Jiangsu Ai Di Pharma Group Co., Ltd. romanizedJiangsu Ai Di Pharma Group Co., Ltd. romanized国药准字H202635362026/03/10See sourceGeneric approved under the new chemical-drug registration classificationCDE
Hetero Labs LimitedHetero Labs Limited国药准字HJ202600232026/02/10See sourceGeneric approved under the new chemical-drug registration classificationCDE
Shanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanizedShanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized国药准字H202556172025/09/30See sourceGeneric approved under the new chemical-drug registration classificationCDE
Qilu Pharmaceutical Co., Ltd.Qilu Pharmaceutical Co., Ltd.国药准字H202341262023/09/05See sourceGeneric approved under the new chemical-drug registration classificationCDE
Anhui Bei Ke Biopharmaceutical Co., Ltd. romanizedAnhui Bei Ke Biopharmaceutical Co., Ltd. romanized国药准字H202663222026/10/20See sourceGeneric 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: 7 distinct approval numbers and 7 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Qilu Pharmaceutical Co., Ltd.国药准字H20234126See sourceNot stated by sourceXJ05AXD255A001010104021NHSA
Shanghai Di Sai Nuo Pharmaceuticals Group Co., Ltd. romanized国药准字H20255617See sourceNot stated by sourceXJ05AXD255A001010105821NHSA
Ao Rui Te Pharma Co., Ltd. romanized国药准字H20264225See sourceNot stated by sourceXJ05AXD255A001010108121NHSA
Hetero Labs Limited国药准字HJ20260023See sourceNot stated by sourceXJ05AXD255A001010179426NHSA
ViiV Healthcare UK LimitedH20150683See sourceNot stated by sourceXJ05AXD255A001010179474NHSA
Jiangsu Ai Di Pharma Group Co., Ltd. romanized国药准字H20263536See sourceNot stated by sourceXJ05AXD255A001010181452NHSA
ViiV Healthcare B.V.国药准字HJ20150683See sourceNot stated by sourceXJ05AXD255A001010279474NHSA

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 2 · Supplement 1

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Dong Bei Pharmaceutical Group Shenyang Di Yi Pharmaceutical Co., Ltd. romanizedCYHS2602412Generic2026/09/24Not stated by sourceCDE
Chengdu Brilliant Pharmaceutical Co., Ltd.CYHS2601019Generic2026/04/30Not stated by sourceCDE
ViiV Healthcare B.V.; Delpharm Poznan S.AJYHB2500595Supplement2025/11/06Not 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
Dong Bei Pharmaceutical Group Shenyang Di Yi Pharmaceutical Co., Ltd. romanizedCYHS2602412Generic2026/09/24Not stated by sourceCDE
Chengdu Brilliant Pharmaceutical Co., Ltd.CYHS2601019Generic2026/04/30Not stated by sourceCDE
API registrations

Non-component matches: 9 companies with A status and 3 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
多替拉韦钠 · No verified English nameDong Bei Pharmaceutical Group Co., Ltd. romanizedY20260000543IExact ingredient2026/07/01CDE
多替拉韦钠 · No verified English nameLaurus Labs LimitedY20250000916IExact ingredient2025/09/18CDE
多替拉韦钠 · No verified English nameSichuan Ren An Pharma Co., Ltd. romanizedY20250000207AExact ingredient2026/07/27CDE
多替拉韦钠 · No verified English nameAnhui Bei Ke Pharmaceutical Co., Ltd. romanizedY20240001543AExact ingredient2026/07/02CDE
多替拉韦钠 · No verified English nameDong Bei Pharmaceutical Group Co., Ltd. romanizedY20240001408IExact ingredient2024/12/20CDE
多替拉韦钠 · No verified English nameChongqing Kai Lin Pharmaceutical Co., Ltd. romanizedY20240000649AExact ingredient2026/03/20CDE
多替拉韦钠 · No verified English nameChongqing Bo Teng Pharmaceutical Technology Co., Ltd. romanizedY20240000525AExact ingredient2026/02/13CDE
多替拉韦钠 · No verified English nameYang Zhou Ai Di Pharmaceuticals Technology Co., Ltd. romanizedY20240000542AExact ingredient2025/10/27CDE
多替拉韦钠 · No verified English nameShanghai Di Sai Nuo Chemical Pharmaceutical Co., Ltd. romanizedY20240000231AExact ingredient2025/09/17CDE
多替拉韦钠 · No verified English nameShijiazhuang Long Ze Pharmaceutical Co., Ltd. romanizedY20240000162AExact ingredient2025/11/14CDE
多替拉韦钠 · No verified English nameYang Zhou Ao Rui Te Pharma Co., Ltd. romanizedY20230001397AExact ingredient2026/05/15CDE
多替拉韦钠 · No verified English nameShandong An Hong Pharmaceutical Co., Ltd. romanizedY20220000041AExact ingredient2023/09/14CDE

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. 2026/10/20Marketing application approved

    Anhui Bei Ke Biopharmaceutical Co., Ltd. romanized

    CYHS2501764 · 国药准字H20266322

    Fact date: 2026/10/20 · Publication date: 2026/10/22 · Site observation date: 2026/11/03

    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 65 ↗
  2. 2026/09/24Accepted

    Dong Bei Pharmaceutical Group Shenyang Di Yi Pharmaceutical Co., Ltd. romanized

    CYHS2602412

    Fact date: 2026/09/24 · 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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