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Milnacipran Hydrochloride Tablets

As of 13 November 2026, for Milnacipran Hydrochloride Tablets, 8 applications are listed as under review at China's CDE; 4 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 3 holders.

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

Listed in the US FDA Orange Book as SAVELLA (NDA 022256, ABBVIE INC).

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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 1 of 1 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
SAVELLA ABBVIE INC NDA 022256 · Product no. 001, 002, 003, 004 TABLET ORAL HUMAN PRESCRIPTION DRUG 2009/01/14

Other dosage forms of the same ingredient

No listings in this group among the displayed brand names.

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: 3 holders; 1 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
Shanghai Shyndec Pharmaceutical Co., Ltd.Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H202471582024/07/1050mgDrug that passed quality-and-efficacy consistency evaluationCDE
Hebei Long Hai Pharma Co., Ltd. romanizedHebei Long Hai Pharma Co., Ltd. romanized国药准字H202435522024/04/2425mgGeneric approved under the new chemical-drug registration classificationCDE
Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanizedSichuan Ke Rui De Pharmaceutical Co., Ltd. romanized国药准字H202345102023/11/2125mgGeneric approved under the new chemical-drug registration classificationCDE
Shanghai Shyndec Pharmaceutical Co., Ltd.Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H201000522022/05/1825mgDrug that passed quality-and-efficacy consistency evaluationCDE
Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanizedSichuan Ke Rui De Pharmaceutical Co., Ltd. romanized国药准字H202692002026/08/1150mgGeneric 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 3 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H2010005225mgCategory BXN06AXM103A001010100814NHSA
Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanized国药准字H2023451025mgCategory BXN06AXM103A001010102181NHSA
Hebei Long Hai Pharma Co., Ltd. romanized国药准字H2024355225mgCategory BXN06AXM103A001010102766NHSA
Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H2010005225mgCategory BXN06AXM103A001010200814NHSA
Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanized国药准字H2023451025mgCategory BXN06AXM103A001010202181NHSA
Hebei Long Hai Pharma Co., Ltd. romanized国药准字H2024355225mgCategory BXN06AXM103A001010202766NHSA
Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H2010005225mgCategory BXN06AXM103A001010300814NHSA
Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H2024715850mgCategory BXN06AXM103A001020100814NHSA
Shanghai Shyndec Pharmaceutical Co., Ltd.国药准字H2024715850mgCategory BXN06AXM103A001020200814NHSA

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: 8 filings and 5 distinct first applicants.

Generic 8

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.CYHS2602329Generic2026/09/18Not stated by sourceCDE
Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.CYHS2602328Generic2026/09/18Not stated by sourceCDE
Hebei Wan Long Pharma Co., Ltd. romanized; Hebei Long Hai Pharma Co., Ltd. romanizedCYHS2601197Generic2026/05/26Not stated by sourceCDE
Hebei Wan Long Pharma Co., Ltd. romanized; Hebei Long Hai Pharma Co., Ltd. romanizedCYHS2601196Generic2026/05/26Not stated by sourceCDE
Shijiazhuang Long Ze Pharmaceutical Co., Ltd. romanizedCYHS2600858Generic2026/04/14Not stated by sourceCDE
Shijiazhuang Long Ze Pharmaceutical Co., Ltd. romanizedCYHS2600857Generic2026/04/14Not stated by sourceCDE
Zhejiang Hua Bei Pharma Co., Ltd. romanized; Le Pu Pharmaceutical Technology Co., Ltd. romanizedCYHS2600586Generic2026/02/28Not stated by sourceCDE
Bai Yun Shandong Tai Shang Qiu Pharma Co., Ltd. romanizedCYHS2503173Generic2025/08/29Not stated by sourceCDE
New generic filings in 2026

Loaded records: 7 filings and 4 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.CYHS2602329Generic2026/09/18Not stated by sourceCDE
Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.CYHS2602328Generic2026/09/18Not stated by sourceCDE
Hebei Wan Long Pharma Co., Ltd. romanized; Hebei Long Hai Pharma Co., Ltd. romanizedCYHS2601197Generic2026/05/26Not stated by sourceCDE
Hebei Wan Long Pharma Co., Ltd. romanized; Hebei Long Hai Pharma Co., Ltd. romanizedCYHS2601196Generic2026/05/26Not stated by sourceCDE
Shijiazhuang Long Ze Pharmaceutical Co., Ltd. romanizedCYHS2600858Generic2026/04/14Not stated by sourceCDE
Shijiazhuang Long Ze Pharmaceutical Co., Ltd. romanizedCYHS2600857Generic2026/04/14Not stated by sourceCDE
Zhejiang Hua Bei Pharma Co., Ltd. romanized; Le Pu Pharmaceutical Technology Co., Ltd. romanizedCYHS2600586Generic2026/02/28Not stated by sourceCDE
API registrations

Non-component matches: 5 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
盐酸米那普仑 · No verified English nameJiangsu Wei Qi Da Pharma Co., Ltd. romanizedY20240001096AExact ingredient2026/02/13CDE
盐酸米那普仑 · No verified English nameLu Zhou Ke Rui De Pharmaceutical Co., Ltd. romanizedY20210000829AExact ingredient2026/06/10CDE
盐酸米那普仑 · No verified English nameGlenmark Life Sciences LimitedY20200000968IExact ingredient2022/08/15CDE
盐酸米那普仑 · No verified English nameHetero Labs LimitedY20190000779AExact ingredient2025/09/30CDE
盐酸米那普仑 · No verified English nameGuo Yao Group Wei Qi Da Pharma Co., Ltd. romanizedY20190021586AExact ingredient2026/07/29CDE
盐酸米那普仑 · No verified English nameShanghai Shyndec Pharmaceutical Co., Ltd.Y20190002147AExact ingredient—CDE

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. 2026/10/27No longer listed under review

    Sichuan Hong Ming Bo Si Pharma Co., Ltd. romanized; Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanized

    CYHB2601849

    Fact date: 2026/10/27 · Site observation date: 2026/10/27

    Accepted: 2026/10/09

    not on the CDE under-review list in this snapshot; NMPA published approval-document delivery for this acceptance number on 2026/10/27 (approval no.: —; approval date: 2026/10/23); this is a supplemental application, not counted as a new marketing approval · NMPA source · row 16

    NMPA · Table row 16 ↗ View source ↗
  2. 2026/10/27No longer listed under review

    Sichuan Hong Ming Bo Si Pharma Co., Ltd. romanized; Sichuan Ke Rui De Pharmaceutical Co., Ltd. romanized

    CYHB2601848

    Fact date: 2026/10/27 · Site observation date: 2026/10/27

    Accepted: 2026/10/09

    not on the CDE under-review list in this snapshot; NMPA published approval-document delivery for this acceptance number on 2026/10/27 (approval no.: —; approval date: 2026/10/23); this is a supplemental application, not counted as a new marketing approval · NMPA source · row 15

    NMPA · Table row 15 ↗ View source ↗
  3. 2026/10/23Supplement delivery

    Sichuan Hong Ming Bo Si Pharma Co., Ltd. romanized

    CYHB2601849

    Fact date: 2026/10/23 · Publication date: 2026/10/27 · Site observation date: 2026/11/03

    Supplemental application; excluded from new marketing approvals.

    View source · Table row 16 ↗
  4. 2026/10/23Supplement delivery

    Sichuan Hong Ming Bo Si Pharma Co., Ltd. romanized

    CYHB2601848

    Fact date: 2026/10/23 · Publication date: 2026/10/27 · Site observation date: 2026/11/03

    Supplemental application; excluded from new marketing approvals.

    View source · Table row 15 ↗
  5. 2026/10/09Accepted
  6. 2026/10/09Accepted
  7. 2026/09/18Accepted

    Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.

    CYHS2602329

    Fact date: 2026/09/18 · Site observation date: 2026/10/22

    View source ↗
  8. 2026/09/18Accepted

    Ningbo Menovo Tiankang Pharmaceutical Co., Ltd.

    CYHS2602328

    Fact date: 2026/09/18 · 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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