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Sign in to subscribeAs of 13 November 2026, for Pregabalin Extended release Tablets, 13 applications are listed as under review at China's CDE; 4 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 0 holders.
Companies, stages and changes, with each record available on this page.
Listed in the US FDA Orange Book as LYRICA CR (NDA 209501, UPJOHN US 2 LLC).
Last 90 days: Accepted: 4 applications
Current coverage may be incomplete
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: Extended release 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.
| Brand name | Applicant (source text) | Application number | Dosage form (source text) | Route (source text) | Marketing status (source text) | Approval date |
|---|---|---|---|---|---|---|
| LYRICA CR | UPJOHN US 2 LLC | NDA 209501 · Product no. 001, 002, 003 | TABLET, EXTENDED RELEASE | ORAL | HUMAN PRESCRIPTION DRUG | 2017/10/11 |
| Brand name | Applicant (source text) | Application number | Dosage form (source text) | Route (source text) | Marketing status (source text) | Approval date |
|---|---|---|---|---|---|---|
| LYRICA | UPJOHN US 2 LLC | NDA 021446 · Product no. 001, 002, 003, 004, 005, 006, 007, 008 | CAPSULE | ORAL | HUMAN PRESCRIPTION DRUG | 2004/12/30 |
| LYRICA | UPJOHN US 2 LLC | NDA 022488 · Product no. 001 | SOLUTION | ORAL | HUMAN PRESCRIPTION DRUG | 2010/01/04 |
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.
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.
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 holder | Manufacturer | Approval number | Approved | Strength / specification | Catalogue 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.
Loaded records: 3 distinct approval numbers and 1 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210041 | 82.5mg | Category B | XN02BGP112A010010101445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210041 | 82.5mg | Category B | XN02BGP112A010010201445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210042 | 165mg | Category B | XN02BGP112A010020101445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210042 | 165mg | Category B | XN02BGP112A010020201445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210043 | 330mg | Category B | XN02BGP112A010030101445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20210043 | 330mg | Category B | XN02BGP112A010030201445 | NHSA |
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.
Loaded records: 13 filings and 5 distinct first applicants.
Generic 13
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602149 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602148 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602147 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602018 | Generic | 2026/08/14 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602017 | Generic | 2026/08/14 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602016 | Generic | 2026/08/14 | Not stated by source | CDE |
| Hua Run Shuang He Li Min Pharma (Jinan) Co., Ltd. romanized | CYHS2601907 | Generic | 2026/08/05 | Not stated by source | CDE |
| Beijing Tai De Pharmaceutical Co., Ltd. romanized | CYHS2601329 | Generic | 2026/06/08 | Not stated by source | CDE |
| Beijing Tai De Pharmaceutical Co., Ltd. romanized | CYHS2601328 | Generic | 2026/06/08 | Not stated by source | CDE |
| CSPC OUYI PHARMACEUTICAL CO., LTD. | CYHS2502317 | Generic | 2025/06/28 | Not stated by source | CDE |
| CSPC OUYI PHARMACEUTICAL CO., LTD. | CYHS2502316 | Generic | 2025/06/28 | Not stated by source | CDE |
| CSPC OUYI PHARMACEUTICAL CO., LTD. | CYHS2502315 | Generic | 2025/06/28 | Not stated by source | CDE |
| Chongqing De Run Sheng Pharmaceuticals Co., Ltd. romanized; Chongqing Huapont Pharmaceutical Co., Ltd. | CYHS2602684 | Generic | 2026/11/03 | Not stated by source | CDE |
Loaded records: 10 filings and 4 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602149 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602148 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602147 | Generic | 2026/08/27 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602018 | Generic | 2026/08/14 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602017 | Generic | 2026/08/14 | Not stated by source | CDE |
| Yi Chang Ren Fu Pharma Co., Ltd. romanized | CYHS2602016 | Generic | 2026/08/14 | Not stated by source | CDE |
| Hua Run Shuang He Li Min Pharma (Jinan) Co., Ltd. romanized | CYHS2601907 | Generic | 2026/08/05 | Not stated by source | CDE |
| Beijing Tai De Pharmaceutical Co., Ltd. romanized | CYHS2601329 | Generic | 2026/06/08 | Not stated by source | CDE |
| Beijing Tai De Pharmaceutical Co., Ltd. romanized | CYHS2601328 | Generic | 2026/06/08 | Not stated by source | CDE |
| Chongqing De Run Sheng Pharmaceuticals Co., Ltd. romanized; Chongqing Huapont Pharmaceutical Co., Ltd. | CYHS2602684 | Generic | 2026/11/03 | Not stated by source | CDE |
Non-component matches: 25 companies with A status and 9 I-status records. Component matches are listed separately and excluded from these counts.
| Name | Company / applicant | Registration number | Status | Name match | Source update date | View source |
|---|---|---|---|---|---|---|
| 普瑞巴林 · No verified English name | Anhui Ding Wang Pharmaceuticals Co., Ltd. romanized | Y20260000861 | I | Exact ingredient | 2026/10/26 | CDE |
| 普瑞巴林 · No verified English name | Zhejiang Zhu Zi Pharmaceutical Co., Ltd. romanized | Y20260000563 | I | Exact ingredient | 2026/07/16 | CDE |
| 普瑞巴林 · No verified English name | Wan Yang Heng Shui Pharmaceutical Co., Ltd. romanized | Y20250001306 | I | Exact ingredient | 2025/12/04 | CDE |
| 普瑞巴林 · No verified English name | Shandong Li Xin Pharmaceutical Co., Ltd. romanized | Y20250000894 | I | Exact ingredient | 2025/09/30 | CDE |
| 普瑞巴林 · No verified English name | Zhejiang Pu Luo Jia Yuan Pharma Co., Ltd. romanized | Y20250000865 | I | Exact ingredient | 2025/09/03 | CDE |
| 普瑞巴林 · No verified English name | MSN Pharmachem Private Limited | Y20240000210 | A | Exact ingredient | 2026/05/20 | CDE |
| 普瑞巴林 · No verified English name | Upjohn EESV | Y20230001164 | A | Exact ingredient | 2025/12/29 | CDE |
| 普瑞巴林 · No verified English name | Shuang He Pharma (Shang Qiu) Co., Ltd. romanized | Y20230000632 | A | Exact ingredient | 2025/04/07 | CDE |
| 普瑞巴林 · No verified English name | Hikal Limited | Y20220000761 | A | Exact ingredient | 2025/04/22 | CDE |
| 普瑞巴林 · No verified English name | Shandong Li Xin Pharmaceutical Co., Ltd. romanized | Y20220000631 | I | Exact ingredient | 2022/09/08 | CDE |
| 普瑞巴林 · No verified English name | Vasudha Pharma Chem Limited | Y20210000819 | I | Exact ingredient | 2021/12/21 | CDE |
| 普瑞巴林 · No verified English name | Hunan Sai Long Pharma Co., Ltd. romanized | Y20210000955 | A | Exact ingredient | 2024/03/07 | CDE |
| 普瑞巴林 · No verified English name | Dong Bei Pharmaceutical Group Co., Ltd. romanized | Y20210000638 | A | Exact ingredient | 2024/01/24 | CDE |
| 普瑞巴林 · No verified English name | MSN Life Sciences Private Limited Unit - III romanized | Y20200001043 | A | Exact ingredient | 2025/08/16 | CDE |
| 普瑞巴林 · No verified English name | Divi’s Laboratories Limited | Y20210000256 | A | Exact ingredient | 2024/01/17 | CDE |
| 普瑞巴林 · No verified English name | Dr.Reddy‘s Laboratories Limited | Y20210000101 | I | Exact ingredient | 2023/12/20 | CDE |
| 普瑞巴林 · No verified English name | DR. REDDYS LABORATORIES LIMITED | Y20200000823 | A | Exact ingredient | 2026/07/11 | CDE |
| 普瑞巴林 · No verified English name | Jiangsu Hui Ju Pharma Co., Ltd. romanized | Y20190000654 | A | Exact ingredient | 2026/04/24 | CDE |
| 普瑞巴林 · No verified English name | CSPC OUYI PHARMACEUTICAL CO., LTD. | Y20190021404 | A | Exact ingredient | 2026/03/17 | CDE |
| 普瑞巴林 · No verified English name | Shijiazhuang Long Ze Pharmaceutical Co., Ltd. romanized | Y20190021315 | A | Exact ingredient | 2026/04/20 | CDE |
| 普瑞巴林 · No verified English name | Chongqing Sai Wei Pharma Co., Ltd. romanized | Y20190009848 | A | Exact ingredient | — | CDE |
| 普瑞巴林 · No verified English name | Chongqing Sai Wei Pharma Co., Ltd. romanized | Y20190000198 | A | Exact ingredient | 2025/09/25 | CDE |
| 普瑞巴林 · No verified English name | Ao Rui Te Pharma Co., Ltd. romanized | Y20190000368 | A | Exact ingredient | 2026/08/14 | CDE |
| 普瑞巴林 · No verified English name | Zhejiang Tian Yu Pharma Co., Ltd. romanized | Y20180001381 | A | Exact ingredient | 2026/01/13 | CDE |
| 普瑞巴林 · No verified English name | Zhejiang Mei Nuo Hua Drug Chemical Co., Ltd. romanized | Y20180001513 | A | Exact ingredient | 2025/07/18 | CDE |
| 普瑞巴林 · No verified English name | Jiangsu En Hua Pharma Co., Ltd. romanized | Y20170001560 | A | Exact ingredient | 2023/07/14 | CDE |
| 普瑞巴林 · No verified English name | Shuang He Pharma (Shang Qiu) Co., Ltd. romanized | Y20170001559 | A | Exact ingredient | 2023/05/11 | CDE |
| 普瑞巴林 · No verified English name | ZHE JIANG HUA HAI PHARMACEUTICALCO.,LTD. | Y20170001497 | A | Exact ingredient | 2023/08/16 | CDE |
| 普瑞巴林 · No verified English name | Guo Yao Group Yi Bin Pharmaceutical Co., Ltd. romanized | Y20170001200 | A | Exact ingredient | 2024/04/26 | CDE |
| 普瑞巴林 · No verified English name | Hetero Drugs Limited, Unit- IX | Y20170001183 | A | Exact ingredient | 2025/12/06 | CDE |
| 普瑞巴林 · No verified English name | Lang Fang Gao Bo Jing Bang Pharmaceutical Co., Ltd. romanized | Y20170001167 | A | Exact ingredient | 2022/09/08 | CDE |
| 普瑞巴林 · No verified English name | Optimus Drugs Pvt Ltd | Y20170001044 | I | Exact ingredient | — | CDE |
| 普瑞巴林 · No verified English name | SUN PHARMACEUTICAL INDUSTRIES LTD | Y20170000832 | A | Exact ingredient | 2022/09/05 | CDE |
| 普瑞巴林 · No verified English name | Shandong An Hong Pharmaceutical Co., Ltd. romanized | Y20170000821 | A | Exact ingredient | 2026/10/30 | CDE |
| 普瑞巴林 · No verified English name | Alembic Pharmaceuticals Ltd. | Y20170000779 | A | Exact ingredient | 2026/03/19 | CDE |
| 普瑞巴林 · No verified English name | CTX Lifesciences Pvt. Ltd. | Y20170000558 | A | Exact ingredient | 2026/08/22 | 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.
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.
CYHS2602684
Fact date: 2026/11/03 · Site observation date: 2026/11/04
View source ↗CYHS2602149
Fact date: 2026/08/27 · Site observation date: 2026/10/22
View source ↗CYHS2602148
Fact date: 2026/08/27 · Site observation date: 2026/10/22
View source ↗CYHS2602147
Fact date: 2026/08/27 · Site observation date: 2026/10/22
View source ↗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.
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.
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.
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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