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Pregabalin Extended release Tablets(普瑞巴林缓释片)

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

Last 90 days: Accepted: 7 applications

Current coverage may be incomplete

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Complete CDE snapshot
2026/11/10 07:27
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.

Company names, approval identifiers and strengths are retained as recorded in the Chinese sources. Category labels include the original wording for verification.

Chemical-drug catalogue

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

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
No matching records were found in the currently loaded source data; coverage dates are listed below.

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: 3 distinct approval numbers and 1 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
江苏恒瑞医药股份有限公司 国药准字H20210041 82.5mg Category B (乙) XN02BGP112A010010101445NHSA
江苏恒瑞医药股份有限公司 国药准字H20210041 82.5mg Category B (乙) XN02BGP112A010010201445NHSA
江苏恒瑞医药股份有限公司 国药准字H20210042 165mg Category B (乙) XN02BGP112A010020101445NHSA
江苏恒瑞医药股份有限公司 国药准字H20210042 165mg Category B (乙) XN02BGP112A010020201445NHSA
江苏恒瑞医药股份有限公司 国药准字H20210043 330mg Category B (乙) XN02BGP112A010030101445NHSA
江苏恒瑞医药股份有限公司 国药准字H20210043 330mg Category B (乙) XN02BGP112A010030201445NHSA

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: 13 filings and 5 distinct first applicants.

Generic 13

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
宜昌人福药业有限责任公司 CYHS2602149 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602148 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602147 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602018 Generic2026/08/14Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602017 Generic2026/08/14Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602016 Generic2026/08/14Not stated by sourceCDE
华润双鹤利民药业(济南)有限公司 CYHS2601907 Generic2026/08/05Not stated by sourceCDE
北京泰德制药股份有限公司 CYHS2601329 Generic2026/06/08Not stated by sourceCDE
北京泰德制药股份有限公司 CYHS2601328 Generic2026/06/08Not stated by sourceCDE
石药集团欧意药业有限公司 CYHS2502317 Generic2025/06/28Not stated by sourceCDE
石药集团欧意药业有限公司 CYHS2502316 Generic2025/06/28Not stated by sourceCDE
石药集团欧意药业有限公司 CYHS2502315 Generic2025/06/28Not stated by sourceCDE
重庆德润笙医药有限公司;重庆华邦制药有限公司 CYHS2602684 Generic2026/11/03Not stated by sourceCDE
New generic filings in 2026

Loaded records: 10 filings and 4 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
宜昌人福药业有限责任公司 CYHS2602149 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602148 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602147 Generic2026/08/27Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602018 Generic2026/08/14Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602017 Generic2026/08/14Not stated by sourceCDE
宜昌人福药业有限责任公司 CYHS2602016 Generic2026/08/14Not stated by sourceCDE
华润双鹤利民药业(济南)有限公司 CYHS2601907 Generic2026/08/05Not stated by sourceCDE
北京泰德制药股份有限公司 CYHS2601329 Generic2026/06/08Not stated by sourceCDE
北京泰德制药股份有限公司 CYHS2601328 Generic2026/06/08Not stated by sourceCDE
重庆德润笙医药有限公司;重庆华邦制药有限公司 CYHS2602684 Generic2026/11/03Not stated by sourceCDE
API registrations

Non-component matches: 25 companies with A status and 9 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
普瑞巴林安徽鼎旺医药有限公司Y20260000861IExact ingredient2026/10/26CDE
普瑞巴林浙江竹子制药有限公司Y20260000563IExact ingredient2026/07/16CDE
普瑞巴林万洋衡水制药有限公司Y20250001306IExact ingredient2025/12/04CDE
普瑞巴林山东立新制药有限公司Y20250000894IExact ingredient2025/09/30CDE
普瑞巴林浙江普洛家园药业有限公司Y20250000865IExact ingredient2025/09/03CDE
普瑞巴林MSN Pharmachem Private LimitedY20240000210AExact ingredient2026/05/20CDE
普瑞巴林Upjohn EESVY20230001164AExact ingredient2025/12/29CDE
普瑞巴林双鹤药业(商丘)有限责任公司Y20230000632AExact ingredient2025/04/07CDE
普瑞巴林Hikal LimitedY20220000761AExact ingredient2025/04/22CDE
普瑞巴林山东立新制药有限公司Y20220000631IExact ingredient2022/09/08CDE
普瑞巴林Vasudha Pharma Chem LimitedY20210000819IExact ingredient2021/12/21CDE
普瑞巴林湖南赛隆药业有限公司Y20210000955AExact ingredient2024/03/07CDE
普瑞巴林东北制药集团股份有限公司Y20210000638AExact ingredient2024/01/24CDE
普瑞巴林MSN Life Sciences Private Limited Unit-ⅢY20200001043AExact ingredient2025/08/16CDE
普瑞巴林Divi’s Laboratories LimitedY20210000256AExact ingredient2024/01/17CDE
普瑞巴林Dr.Reddy‘s Laboratories LimitedY20210000101IExact ingredient2023/12/20CDE
普瑞巴林DR. REDDYS LABORATORIES LIMITEDY20200000823AExact ingredient2026/07/11CDE
普瑞巴林江苏慧聚药业股份有限公司Y20190000654AExact ingredient2026/04/24CDE
普瑞巴林石药集团欧意药业有限公司Y20190021404AExact ingredient2026/03/17CDE
普瑞巴林石家庄龙泽制药股份有限公司Y20190021315AExact ingredient2026/04/20CDE
普瑞巴林重庆赛维药业有限公司Y20190009848AExact ingredient—CDE
普瑞巴林重庆赛维药业有限公司Y20190000198AExact ingredient2025/09/25CDE
普瑞巴林奥锐特药业股份有限公司Y20190000368AExact ingredient2026/08/14CDE
普瑞巴林浙江天宇药业股份有限公司Y20180001381AExact ingredient2026/01/13CDE
普瑞巴林浙江美诺华药物化学有限公司Y20180001513AExact ingredient2025/07/18CDE
普瑞巴林江苏恩华药业股份有限公司Y20170001560AExact ingredient2023/07/14CDE
普瑞巴林双鹤药业(商丘)有限责任公司Y20170001559AExact ingredient2023/05/11CDE
普瑞巴林浙江华海药业股份有限公司Y20170001497AExact ingredient2023/08/16CDE
普瑞巴林国药集团宜宾制药有限责任公司Y20170001200AExact ingredient2024/04/26CDE
普瑞巴林Hetero Drugs Limited, Unit- IXY20170001183AExact ingredient2025/12/06CDE
普瑞巴林廊坊高博京邦制药有限公司Y20170001167AExact ingredient2022/09/08CDE
普瑞巴林Optimus Drugs Pvt LtdY20170001044IExact ingredient—CDE
普瑞巴林SUN PHARMACEUTICAL INDUSTRIES LTDY20170000832AExact ingredient2022/09/05CDE
普瑞巴林山东安弘制药有限公司Y20170000821AExact ingredient2026/10/30CDE
普瑞巴林Alembic Pharmaceuticals Ltd.Y20170000779AExact ingredient2026/03/19CDE
普瑞巴林CTX Lifesciences Pvt. Ltd.Y20170000558AExact ingredient2026/08/22CDE

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: 2026/11/10 07:23. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.

  1. 2026/11/03Accepted

    重庆德润笙医药有限公司;重庆华邦制药有限公司

    CYHS2602684

    Fact date: 2026/11/03 · Site observation date: 2026/11/04

    View source ↗
  2. 2026/08/27Accepted

    宜昌人福药业有限责任公司

    CYHS2602149

    Fact date: 2026/08/27 · Site observation date: 2026/10/22

    View source ↗
  3. 2026/08/27Accepted

    宜昌人福药业有限责任公司

    CYHS2602148

    Fact date: 2026/08/27 · Site observation date: 2026/10/22

    View source ↗
  4. 2026/08/27Accepted

    宜昌人福药业有限责任公司

    CYHS2602147

    Fact date: 2026/08/27 · Site observation date: 2026/10/22

    View source ↗
  5. 2026/08/14Accepted

    宜昌人福药业有限责任公司

    CYHS2602018

    Fact date: 2026/08/14 · Site observation date: 2026/10/22

    View source ↗
  6. 2026/08/14Accepted

    宜昌人福药业有限责任公司

    CYHS2602017

    Fact date: 2026/08/14 · Site observation date: 2026/10/22

    View source ↗
  7. 2026/08/14Accepted

    宜昌人福药业有限责任公司

    CYHS2602016

    Fact date: 2026/08/14 · Site observation date: 2026/10/22

    View source ↗

How current is each source?

CDE acceptances and review
Last successful update: 2026/11/10 07:27
Chemical-drug catalogue
Last successful update: 2026/11/10 07:23

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: 2026/11/10 07:25
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: 2026/11/10 18:31

First index-page publication dates: 2026-10-26 to 2026-11-10; 0 pages pending. Covers loaded notices only, not a complete historical approval database.

Drug Clinical Trial Registry and Information Disclosure Platform
Last successful update: 2026/11/10 08:10 · 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: 3/30; discovered pending details: 20. 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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