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Salmeterol Xinafoate and Fluticasone Propionate Powder for Inhalation(沙美特罗替卡松吸入粉雾剂)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 1 applicationNo longer listed under review: 1 applicationSupplement delivery: 1 application
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 holders0View records ↓
Under-review filings12View records ↓
This year’s generic filers2View records ↓
NHSA approval numbers11View records ↓
API companies with A status0View records ↓
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 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.
NHSA drug codes
Loaded records: 11 distinct approval numbers and 6 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Laboratoire GlaxoSmithKline | 国药准字HJ20150323 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031010178564 | NHSA |
| M/s. Cipla Limited | 国药准字HJ20250075 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031010179537 | NHSA |
| 四川普锐特药业有限公司 | 国药准字H20253521 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙酸氟替卡松250μg,递送剂量为昔萘酸沙美特罗47µg(按C₂₅H₃₇NO₄计)与丙酸氟替卡松231µg | Category B (乙) | XR03AKS054L031010181590 | NHSA |
| 健康元药业集团股份有限公司 | 国药准字H20243906 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031010183037 | NHSA |
| 上海欧米尼医药科技有限公司 | 国药准字H20255235 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙酸氟替卡松250μg ;递送剂量为昔萘酸沙美特罗47μg(按C₂₅H₃₇NO₄计)与丙酸氟替卡松231μg | Category B (乙) | XR03AKS054L031010185001 | NHSA |
| Neutec Ilac San. Tic. A.S. | 国药准字HJ20240136 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计) 与 | Category B (乙) | XR03AKS054L031010185370 | NHSA |
| Laboratoire GlaxoSmithKline | 国药准字HJ20150324 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031010278564 | NHSA |
| Laboratoire GlaxoSmithKline | 国药准字HJ20150325 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031020178564 | NHSA |
| M/s. Cipla Limited | 国药准字HJ20250076 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031020179537 | NHSA |
| Neutec Ilac San. Tic. A.S. | 国药准字HJ20240137 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计) 与 | Category B (乙) | XR03AKS054L031020185370 | NHSA |
| Laboratoire GlaxoSmithKline | 国药准字HJ20150323 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031020278564 | NHSA |
| Laboratoire GlaxoSmithKline | 国药准字HJ20150324 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031020378564 | NHSA |
| Laboratoire GlaxoSmithKline | 国药准字HJ20150325 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031020478564 | NHSA |
| M/s. Cipla Limited | 国药准字HJ20250077 | 每泡含昔萘酸沙美特罗50μg(按C₂₅H₃₇NO₄计)与丙 | Category B (乙) | XR03AKS054L031030179537 | 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: 12 filings and 5 distinct first applicants.
Generic 3 · Import 2 · Supplement 7
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 博瑞制药（苏州）有限公司 | CYHS2600253 | Generic | 2026/01/22 | Not stated by source | CDE |
| 博瑞制药（苏州）有限公司 | CYHS2600252 | Generic | 2026/01/22 | Not stated by source | CDE |
| Celon Pharma S.A.;Jiangsu Simcere Pharmaceutical Co. Ltd. | JYHS2400054 | Import | 2024/10/30 | Not stated by source | CDE |
| Celon Pharma S.A.;Jiangsu Simcere Pharmaceutical Co. Ltd. | JYHS2400053 | Import | 2024/10/30 | Not stated by source | CDE |
| 润生药业有限公司 | CYHS2602496 | Generic | 2026/10/12 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2600460 | Supplement | 2026/08/12 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2600459 | Supplement | 2026/08/12 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2600458 | Supplement | 2026/08/12 | Not stated by source | CDE |
| 四川普锐特药业有限公司 | CYHB2600789 | Supplement | 2026/04/22 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2500545 | Supplement | 2025/10/17 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2500544 | Supplement | 2025/10/17 | Not stated by source | CDE |
| Laboratoire GlaxoSmithKline;Glaxo Wellcome Production | JYHB2500543 | Supplement | 2025/10/17 | Not stated by source | CDE |
New generic filings in 2026
Loaded records: 3 filings and 2 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 博瑞制药（苏州）有限公司 | CYHS2600253 | Generic | 2026/01/22 | Not stated by source | CDE |
| 博瑞制药（苏州）有限公司 | CYHS2600252 | Generic | 2026/01/22 | Not stated by source | CDE |
| 润生药业有限公司 | CYHS2602496 | Generic | 2026/10/12 | Not stated by source | CDE |
API registrations
Non-component matches: 0 companies with A status and 0 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 |
|---|---|---|---|---|---|---|
| No matching records were found in the currently loaded source data; coverage dates are listed below. | ||||||
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.
-
2026/10/23No longer listed under review
四川普锐特药业有限公司
CYHB2600788
Fact date: 2026/10/23 · Site observation date: 2026/10/23
Accepted: 2026/04/22
not on the CDE under-review list in this snapshot; NMPA published approval-document delivery for this acceptance number on 2026/10/23 (approval no.: —; approval date: 2026/10/21); this is a supplemental application, not counted as a new marketing approval · NMPA source · row 12
NMPA · Table row 12 ↗ View source ↗ -
2026/10/21Supplement delivery
四川普锐特药业有限公司
CYHB2600788
Fact date: 2026/10/21 · Publication date: 2026/10/23 · Site observation date: 2026/11/03
Supplemental application; excluded from new marketing approvals.
View source · Table row 12 ↗ -
2026/10/12Accepted
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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