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Letermovir Tablets(来特莫韦片)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 1 applicationNo longer listed under review: 1 applicationSupplement delivery: 2 applications
Current coverage may be incomplete
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.
Catalogue holders5View records ↓
Under-review filings6View records ↓
This year’s generic filers3View records ↓
NHSA approval numbers7View records ↓
API companies with A status8View records ↓
Chemical-drug catalogue
Loaded records: 5 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 5 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 |
|---|---|---|---|---|---|---|
| 江西迪赛诺医药集团有限公司 | 江西迪赛诺医药集团有限公司 | 国药准字H20265547 | 2026/08/04 | 240mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 浙江海正药业股份有限公司 | 浙江海正药业股份有限公司 | 国药准字H20265140 | 2026/07/08 | 0.24g | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 齐鲁制药有限公司 | 齐鲁制药有限公司 | 国药准字H20256071 | 2025/11/25 | 240mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 重庆希韦医药科技有限公司 | 重庆博腾药业有限公司 | 国药准字H20254189 | 2025/05/20 | 240mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
| 南京正大天晴制药有限公司 | 南京正大天晴制药有限公司 | 国药准字H20243449 | 2024/04/07 | 240mg | Generic approved under the new chemical-drug registration classification (按化学药品新注册分类批准的仿制药) | CDE |
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 6 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| 南京正大天晴制药有限公司 | 国药准字H20243449 | 240mg | Category B (乙) | XJ05AXL400A001010101606 | NHSA |
| 齐鲁制药有限公司 | 国药准字H20256071 | 240mg | Category B (乙) | XJ05AXL400A001010104021 | NHSA |
| 浙江海正药业股份有限公司 | 国药准字H20265140 | 0.24g | Category B (乙) | XJ05AXL400A001010104641 | NHSA |
| Merck Sharp & Dohme B.V. | 国药准字HJ20210085 | 240mg | Category B (乙) | XJ05AXL400A001010179325 | NHSA |
| 重庆希韦医药科技有限公司 | 国药准字H20254189 | 240mg | Category B (乙) | XJ05AXL400A001010184682 | NHSA |
| 江西迪赛诺医药集团有限公司 | 国药准字H20265547 | 240mg | Category B (乙) | XJ05AXL400A001010185211 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20243449 | 240mg | Category B (乙) | XJ05AXL400A001010201606 | NHSA |
| 浙江海正药业股份有限公司 | 国药准字H20265140 | 0.24g | Category B (乙) | XJ05AXL400A001010204641 | NHSA |
| 重庆希韦医药科技有限公司 | 国药准字H20254189 | 240mg | Category B (乙) | XJ05AXL400A001010284682 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20243449 | 240mg | Category B (乙) | XJ05AXL400A001010301606 | NHSA |
| Merck Sharp & Dohme B.V. | 国药准字HJ20210086 | 480mg | Category B (乙) | XJ05AXL400A001020179325 | 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.
Current under-review applications
Loaded records: 6 filings and 6 distinct first applicants.
Generic 6
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 山东鲁抗医药股份有限公司 | CYHS2600847 | Generic | 2026/04/13 | Not stated by source | CDE |
| 旺山旺水（连云港）制药有限公司 | CYHS2600650 | Generic | 2026/03/12 | Not stated by source | CDE |
| 上海上药信谊药厂有限公司 | CYHS2602303 | Generic | 2026/09/16 | Not stated by source | CDE |
| 宜昌人福药业有限责任公司 | CYHS2503589 | Generic | 2025/09/30 | Not stated by source | CDE |
| 海南合瑞制药股份有限公司 | CYHS2503046 | Generic | 2025/08/19 | Not stated by source | CDE |
| 华北制药股份有限公司 | CYHS2503032 | Generic | 2025/08/19 | Not stated by source | CDE |
New generic filings in 2026
Loaded records: 3 filings and 3 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 山东鲁抗医药股份有限公司 | CYHS2600847 | Generic | 2026/04/13 | Not stated by source | CDE |
| 旺山旺水（连云港）制药有限公司 | CYHS2600650 | Generic | 2026/03/12 | Not stated by source | CDE |
| 上海上药信谊药厂有限公司 | CYHS2602303 | Generic | 2026/09/16 | Not stated by source | CDE |
API registrations
Non-component matches: 8 companies with A status and 5 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 |
|---|---|---|---|---|---|---|
| 来特莫韦 | 山东特珐曼药业有限公司 | Y20250001286 | I | Exact ingredient | 2025/12/12 | CDE |
| 来特莫韦 | 宜昌天睿生物医药有限责任公司 | Y20250000919 | I | Exact ingredient | 2025/09/02 | CDE |
| 来特莫韦 | 海南合瑞制药股份有限公司 | Y20250000746 | I | Exact ingredient | 2025/07/31 | CDE |
| 来特莫韦 | 山东鲁抗医药股份有限公司 | Y20250000637 | I | Exact ingredient | 2025/07/07 | CDE |
| 来特莫韦 | 河北安健成益医药科技有限公司 | Y20240000795 | A | Exact ingredient | 2026/08/07 | CDE |
| 来特莫韦 | 浙江海正药业股份有限公司 | Y20240001247 | A | Exact ingredient | 2026/06/29 | CDE |
| 来特莫韦 | 江苏正济药业股份有限公司 | Y20240000742 | A | Exact ingredient | 2026/04/23 | CDE |
| 来特莫韦 | 上海迪赛诺化学制药有限公司 | Y20240000784 | A | Exact ingredient | 2026/03/20 | CDE |
| 来特莫韦 | 山东安弘制药有限公司 | Y20240000372 | A | Exact ingredient | 2025/10/27 | CDE |
| 来特莫韦 | 山东诚汇双达药业有限公司 | Y20240000270 | A | Exact ingredient | 2026/07/18 | CDE |
| 来特莫韦 | Lupin Manufacturing Solutions Limited | Y20230000163 | I | Exact ingredient | 2024/02/27 | CDE |
| 来特莫韦 | 浙江车头制药股份有限公司 | Y20230001068 | A | Exact ingredient | 2026/06/02 | CDE |
| 来特莫韦 | 精华制药集团南通有限公司 | Y20220000826 | A | Exact ingredient | 2024/03/15 | 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: 2026/11/10 07:23. NHSA records lack approval dates; only an earlier edition or observation establishes precedence.
-
2026/10/31No longer listed under review
南京正大天晴制药有限公司
CYHB2601529
Fact date: 2026/10/31 · Site observation date: 2026/10/31
Accepted: 2026/08/11
not on the CDE under-review list in this snapshot; NMPA published approval-document delivery for this acceptance number on 2026/10/30 (approval no.: —; approval date: 2026/10/29); this is a supplemental application, not counted as a new marketing approval · NMPA source · row 12
NMPA · Table row 12 ↗ View source ↗ -
2026/10/29Supplement delivery
南京正大天晴制药有限公司
CYHB2601529
Fact date: 2026/10/29 · Publication date: 2026/10/30 · Site observation date: 2026/11/03
Supplemental application; excluded from new marketing approvals.
View source · Table row 12 ↗ -
2026/10/20Supplement delivery
重庆希韦医药科技有限公司
CYHB2601470
Fact date: 2026/10/20 · Publication date: 2026/10/21 · Site observation date: 2026/11/03
Supplemental application; excluded from new marketing approvals.
View source · Table row 8 ↗ -
2026/09/16Accepted
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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