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Budesonide Nasal Spray(布地奈德鼻喷雾剂)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 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 holders1View records ↓
Under-review filings3View records ↓
This year’s generic filers2View records ↓
NHSA approval numbers13View records ↓
API companies with A status21View records ↓
Chemical-drug catalogue
Loaded records: 1 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 |
|---|---|---|---|---|---|---|
| McNeil Sweden AB | AstraZeneca AB | H20171309;H20171310 | 2002/02/21 | 每瓶120喷，每喷含布地奈德32μg，药液浓度为0.64mg/ml | Imported originator drug (进口原研药品) | CDE |
| McNeil Sweden AB | AstraZeneca AB | H20171311;H20171312 | 2002/02/21 | 每瓶120喷，每喷含布地奈德64μg，药液浓度为1.28mg/ml | Imported originator drug (进口原研药品) | 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: 13 distinct approval numbers and 4 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| McNeil Sweden AB | 国药准字J20180024 | 每瓶120喷,每喷含布地奈德32μg,药液浓度为0.64mg/ml | Category B (乙) | XR01ADB165L025010100734 | NHSA |
| 远大九和(江西)药业有限公司 | 国药准字H20234500 | 6ml:7.68mg,120喷,每喷64μg | Category B (乙) | XR01ADB165L025010105402 | NHSA |
| 台湾海默尼药业有限公司 | 国药准字J20190031 | 6ml:7.68mg,64μg/喷 | Category B (乙) | XR01ADB165L025010110427 | NHSA |
| McNeil Sweden AB | 国药准字HJ20171309 | 每瓶120喷,每喷含布地奈德32μg,药液浓度为0.64mg/ml | Category B (乙) | XR01ADB165L025010179321 | NHSA |
| 四川普锐特药业有限公司 | 国药准字H20234511 | 6ml:3.84mg,120喷,每喷32μg | Category B (乙) | XR01ADB165L025010181590 | NHSA |
| 台湾海默尼药业有限公司 | 国药准字HC20181007 | 6ml:7.68mg;64μg/喷 | Category B (乙) | XR01ADB165L025010182195 | NHSA |
| McNeil Sweden AB | H20171310 | 每瓶120喷,每喷含布地奈德32μg,药液浓度为0.64mg/ml | Category B (乙) | XR01ADB165L025010279321 | NHSA |
| 台湾海默尼药业有限公司 | 国药准字HC20191008 | 6ml:7.68mg;64μg/喷 | Category B (乙) | XR01ADB165L025010282195 | NHSA |
| McNeil Sweden AB | 国药准字J20180023 | 每瓶120喷,每喷含布地奈德64μg,药液浓度为1.28mg/ml | Category B (乙) | XR01ADB165L025020100734 | NHSA |
| 远大九和(江西)药业有限公司 | 国药准字H20234507 | 6ml:3.84mg,120喷,每喷32μg | Category B (乙) | XR01ADB165L025020105402 | NHSA |
| 台湾海默尼药业有限公司 | 国药准字J20190031 | 6ml:7.68mg,64μg/喷 | Category B (乙) | XR01ADB165L025020110427 | NHSA |
| McNeil Sweden AB | 国药准字HJ20171311 | 每瓶120喷,每喷含布地奈德64μg,药液浓度为1.28mg/ml | Category B (乙) | XR01ADB165L025020179321 | NHSA |
| 四川普锐特药业有限公司 | 国药准字H20234512 | 6ml:7.68mg,120喷,每喷64μg | Category B (乙) | XR01ADB165L025020181590 | NHSA |
| 台湾海默尼药业有限公司 | 国药准字HC20181007 | 6ml:7.68mg;64μg/喷 | Category B (乙) | XR01ADB165L025020182195 | NHSA |
| McNeil Sweden AB | H20171312 | 每瓶120喷,每喷含布地奈德64μg,药液浓度为1.28mg/ml | Category B (乙) | XR01ADB165L025020279321 | 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: 3 filings and 2 distinct first applicants.
Generic 3
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 山东京卫制药有限公司 | CYHS2602441 | Generic | 2026/10/08 | Not stated by source | CDE |
| 长风药业股份有限公司 | CYHS2600273 | Generic | 2026/01/24 | Not stated by source | CDE |
| 长风药业股份有限公司 | CYHS2600272 | Generic | 2026/01/24 | 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 |
|---|---|---|---|---|---|
| 山东京卫制药有限公司 | CYHS2602441 | Generic | 2026/10/08 | Not stated by source | CDE |
| 长风药业股份有限公司 | CYHS2600273 | Generic | 2026/01/24 | Not stated by source | CDE |
| 长风药业股份有限公司 | CYHS2600272 | Generic | 2026/01/24 | Not stated by source | CDE |
API registrations
Non-component matches: 21 companies with A status and 8 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 |
|---|---|---|---|---|---|---|
| 布地奈德 | 徐州万邦金桥制药有限公司 | Y20260000850 | I | Exact ingredient | 2026/10/14 | CDE |
| 布地奈德 | 奥锐特药业股份有限公司 | Y20250000390 | A | Exact ingredient | 2026/10/14 | CDE |
| 布地奈德 | 浙江神洲药业有限公司 | Y20250000179 | A | Exact ingredient | 2026/09/29 | CDE |
| 布地奈德 | 四川仁安药业有限责任公司 | Y20240000238 | A | Exact ingredient | 2025/07/25 | CDE |
| 布地奈德 | Aspen Oss B.V. | Y20230000013 | A | Exact ingredient | 2025/08/06 | CDE |
| 布地奈德 | 新乡海滨药业有限公司 | Y20220001161 | A | Exact ingredient | 2024/05/29 | CDE |
| 布地奈德 | 博泽格霖（山东）药业有限公司 | Y20220001042 | A | Exact ingredient | 2026/07/08 | CDE |
| 布地奈德 | 博泽格霖（山东）药业有限公司 | Y20220001041 | A | Exact ingredient | 2024/12/27 | CDE |
| 布地奈德 | 山东斯瑞药业有限公司 | Y20220000980 | A | Exact ingredient | 2026/08/22 | CDE |
| 布地奈德 | 河北创健药业有限公司 | Y20220000613 | A | Exact ingredient | 2024/04/25 | CDE |
| 布地奈德 | 新乡海滨药业有限公司 | Y20220000235 | A | Exact ingredient | 2024/01/16 | CDE |
| 布地奈德 | INDUSTRIALE CHIMICA SRL | Y20220000028 | A | Exact ingredient | 2025/01/28 | CDE |
| 布地奈德 | FARMABIOS S.P.A. | Y20210001146 | A | Exact ingredient | 2024/12/31 | CDE |
| 布地奈德 | FARMABIOS S.P.A. | Y20210000328 | I | Exact ingredient | 2021/10/27 | CDE |
| 布地奈德 | Avik Pharmaceutical Ltd | Y20210000776 | A | Exact ingredient | 2025/01/15 | CDE |
| 布地奈德 | Sicor Societa’ Italiana Corticosteroidi S.R.L. | Y20210000494 | I | Exact ingredient | 2021/07/23 | CDE |
| 布地奈德 | Newchem S.p.A. | Y20200001161 | A | Exact ingredient | 2025/06/21 | CDE |
| 布地奈德 | 河南利华制药有限公司 | Y20200001406 | A | Exact ingredient | 2024/02/24 | CDE |
| 布地奈德 | SICOR DE MEXICO, S.A. de C.V. | Y20210000111 | I | Exact ingredient | 2023/07/04 | CDE |
| 布地奈德 | 湖北葛店人福药业有限责任公司 | Y20190009886 | A | Exact ingredient | 2024/09/03 | CDE |
| 布地奈德 | 津药药业股份有限公司 | Y20190008852 | A | Exact ingredient | 2026/01/24 | CDE |
| 布地奈德 | 鲁南贝特制药有限公司 | Y20190003690 | A | Exact ingredient | 2025/03/11 | CDE |
| 布地奈德 | 上海信谊百路达药业有限公司 | Y20190001490 | A | Exact ingredient | 2025/01/23 | CDE |
| 布地奈德 | CURIA SPAIN S.A.U. | Y20190000645 | I | Exact ingredient | 2023/11/20 | CDE |
| 布地奈德 | CURIA SPAIN S.A.U. | Y20190000457 | I | Exact ingredient | 2022/06/22 | CDE |
| 布地奈德 | MINAKEM | Y20180001668 | A | Exact ingredient | 2026/06/13 | CDE |
| 布地奈德 | Aspen Oss B.V. | Y20180001131 | I | Exact ingredient | 2018/12/27 | CDE |
| 布地奈德 | 湖北葛店人福药业有限责任公司 | Y20180000713 | I | Exact ingredient | 2018/07/25 | CDE |
| 布地奈德 | 山东锐顺药业有限公司 | Y20170001463 | A | Exact ingredient | 2025/04/16 | CDE |
| 布地奈德 | VAMSI LABS LTD. | Y20170000975 | A | Exact ingredient | 2025/07/20 | CDE |
| 布地奈德 | 连云港润众制药有限公司 | Y20170000971 | A | Exact ingredient | 2023/03/24 | 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.
-
2026/10/08Accepted
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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