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Sign in to subscribeAs of 13 November 2026, for Fluticasone Propionate Cream, 12 applications are listed as under review at China's CDE; 2 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.
Last 90 days: Accepted: 2 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 5 of 11 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: Cream. 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.
No listings in this group among the displayed brand names.
| Brand name | Applicant (source text) | Application number | Dosage form (source text) | Route (source text) | Marketing status (source text) | Approval date |
|---|---|---|---|---|---|---|
| FLOVENT DISKUS 100 | GLAXO GROUP LTD ENGLAND DBA GLAXOSMITHKLINE | NDA 020833 · Product no. 002 | POWDER | INHALATION | HUMAN PRESCRIPTION DRUG | 2000/09/29 |
| FLOVENT DISKUS 250 | GLAXO GROUP LTD ENGLAND DBA GLAXOSMITHKLINE | NDA 020833 · Product no. 003 | POWDER | INHALATION | HUMAN PRESCRIPTION DRUG | 2000/09/29 |
| FLOVENT DISKUS 50 | GLAXO GROUP LTD ENGLAND DBA GLAXOSMITHKLINE | NDA 020833 · Product no. 001 | POWDER | INHALATION | HUMAN PRESCRIPTION DRUG | 2000/09/29 |
| FLOVENT HFA | GLAXO GROUP LTD DBA GLAXOSMITHKLINE | NDA 021433 · Product no. 001, 002, 003 | AEROSOL, METERED | INHALATION | HUMAN PRESCRIPTION DRUG | 2004/05/14 |
| FLONASE ALLERGY RELIEF | HALEON US HOLDINGS LLC | NDA 205434 · Product no. 001 | SPRAY, METERED | NASAL | HUMAN OTC DRUG | 2014/07/23 |
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: 12 distinct approval numbers and 11 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Chongqing Huapont Pharmaceutical Co., Ltd. | 国药准字H20254589 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002010101003 | NHSA |
| Hubei Heng An Fu Lin Pharma Co., Ltd. romanized | 国药准字H20103501 | 0.05% | Category B | XD07ACF095F002010101808 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002010101955 | NHSA |
| Hebei Xin Zhang Yao Co., Ltd. romanized | 国药准字H20264344 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002010102673 | NHSA |
| Zhejiang San Sheng Man Di Pharma Co., Ltd. romanized | 国药准字H20173270 | 0.05% | Category B | XD07ACF095F002010104726 | NHSA |
| Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanized | 国药准字H20103337 | 0.05% | Category B | XD07ACF095F002010104735 | NHSA |
| Ao Mei Pharmaceutical Factory romanized | 国药准字HC20150021 | 0.05%[(1)5g:2.5mg;(2)10g:5mg;(3)15g:7.5mg | Category B | XD07ACF095F002010179136 | NHSA |
| Glaxo Wellcome UK Limited | H20130431 | 15g:7.5mg(0.05%) | Category B | XD07ACF095F002010179536 | NHSA |
| Fu Yuan Pharma Co., Ltd. romanized | 国药准字H20244439 | 0.05%(15g∶7.5mg) | Category B | XD07ACF095F002010180651 | NHSA |
| Jiangsu Ziyond Pharmaceutical Co., Ltd. | 国药准字H20253814 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002010181475 | NHSA |
| Hubei Heng An Fu Lin Pharma Co., Ltd. romanized | 国药准字H20103501 | 0.05% | Category B | XD07ACF095F002020101808 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002020101955 | NHSA |
| Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanized | 国药准字H20103337 | 0.05% | Category B | XD07ACF095F002020104735 | NHSA |
| Ao Mei Pharmaceutical Factory Co., Ltd. romanized | 国药准字HC20150022 | 0.05%[(1)5g:2.5mg;(2)10g:5mg;(3)15g:7.5mg;(4)20g: | Category B | XD07ACF095F002020179136 | NHSA |
| Fu Yuan Pharma Co., Ltd. romanized | 国药准字H20258213 | 0.05%(20g∶10mg) | Category B | XD07ACF095F002020180651 | NHSA |
| Hubei Heng An Fu Lin Pharma Co., Ltd. romanized | 国药准字H20103501 | 0.05% | Category B | XD07ACF095F002030101808 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002030101955 | NHSA |
| Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanized | 国药准字H20103337 | 0.05% | Category B | XD07ACF095F002030104735 | NHSA |
| Ao Mei Pharmaceutical Factory romanized | 国药准字HC20150021 | 0.05%[(1)5g:2.5mg;(2)10g:5mg;(3)15g:7.5mg | Category B | XD07ACF095F002030179136 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002030201955 | NHSA |
| Hubei Heng An Fu Lin Pharma Co., Ltd. romanized | 国药准字H20103501 | 0.05% | Category B | XD07ACF095F002040101808 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002040101955 | NHSA |
| Ao Mei Pharmaceutical Factory Co., Ltd. romanized | 国药准字HC20150022 | 0.05%[(1)5g:2.5mg;(2)10g:5mg;(3)15g:7.5mg;(4)20g: | Category B | XD07ACF095F002040179136 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002050101955 | NHSA |
| Ao Mei Pharmaceutical Factory Co., Ltd. romanized | 国药准字HC20150022 | 0.05%[(1)5g:2.5mg;(2)10g:5mg;(3)15g:7.5mg;(4)20g: | Category B | XD07ACF095F002050179136 | NHSA |
| Wuhan Nuo An Pharma Co., Ltd. romanized | 国药准字H20173346 | 0.05%(15g:7.5mg) | Category B | XD07ACF095F002060101955 | 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: 12 filings and 10 distinct first applicants.
Supplement 2 · Generic 10
Loaded records: 3 filings and 2 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Zhejiang Gao Zhi Pharmaceuticals Technology Co., Ltd. romanized; Zhejiang Sai Mo Pharmaceutical Co., Ltd. romanized | CYHS2600577 | Generic | 2026/02/28 | Not stated by source | CDE |
| Guangdong Ren Xiang Pharma Co., Ltd. romanized; Zhejiang Sai Mo Pharmaceutical Co., Ltd. romanized | CYHS2600360 | Generic | 2026/02/04 | Not stated by source | CDE |
| Guangdong Ren Xiang Pharma Co., Ltd. romanized; Zhejiang Sai Mo Pharmaceutical Co., Ltd. romanized | CYHS2600359 | Generic | 2026/02/04 | Not stated by source | CDE |
Non-component matches: 18 companies with A status and 7 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 |
|---|---|---|---|---|---|---|
| 丙酸氟替卡松 · No verified English name | Glaxo Operations UK Limited | Y20260000761 | I | Exact ingredient | 2026/09/02 | CDE |
| 丙酸氟替卡松 · No verified English name | Curia Spain S.A.U. | Y20240000551 | I | Exact ingredient | 2024/07/17 | CDE |
| 丙酸氟替卡松 · No verified English name | Glaxo Wellcome Manufacturing Pte Ltd | Y20230001274 | A | Exact ingredient | 2025/12/05 | CDE |
| 丙酸氟替卡松 · No verified English name | INDUSTRIALE CHIMICA S.R.L. | Y20230000326 | A | Exact ingredient | 2026/03/07 | CDE |
| 丙酸氟替卡松 · No verified English name | Bo Ze Ge Lin (Shandong) Pharma Co., Ltd. romanized | Y20230000446 | A | Exact ingredient | 2025/04/16 | CDE |
| 丙酸氟替卡松 · No verified English name | CIPLA LIMITED | Y20230000328 | A | Exact ingredient | 2025/12/13 | CDE |
| 丙酸氟替卡松 · No verified English name | VAMSI LABS LTD. | Y20230000256 | A | Exact ingredient | 2025/09/22 | CDE |
| 丙酸氟替卡松 · No verified English name | Henan Li Hua Pharmaceutical Co., Ltd. romanized | Y20200001241 | A | Exact ingredient | 2025/08/01 | CDE |
| 丙酸氟替卡松 · No verified English name | Shandong Si Rui Pharma Co., Ltd. romanized | Y20200000871 | A | Exact ingredient | 2024/05/30 | CDE |
| 丙酸氟替卡松 · No verified English name | Glaxo Wellcome Manufacturing Pte Ltd | Y20200000383 | A | Exact ingredient | 2023/01/04 | CDE |
| 丙酸氟替卡松 · No verified English name | SANOFI CHIMIE | Y20190021448 | I | Exact ingredient | 2020/06/30 | CDE |
| 丙酸氟替卡松 · No verified English name | Sichuan Ren An Pharma Co., Ltd. romanized | Y20200000487 | A | Exact ingredient | 2026/06/08 | CDE |
| 丙酸氟替卡松 · No verified English name | Hovione FarmaCiencia SA | Y20200000007 | I | Exact ingredient | 2023/09/12 | CDE |
| 丙酸氟替卡松 · No verified English name | Jin Yao Pharma Co., Ltd. romanized | Y20190008858 | A | Exact ingredient | 2026/03/21 | CDE |
| 丙酸氟替卡松 · No verified English name | Lian Yun Gang Run Zhong Pharmaceutical Co., Ltd. romanized | Y20190007593 | A | Exact ingredient | 2024/06/06 | CDE |
| 丙酸氟替卡松 · No verified English name | Ao Rui Te Pharma Co., Ltd. romanized | Y20190007020 | A | Exact ingredient | 2022/10/28 | CDE |
| 丙酸氟替卡松 · No verified English name | Aarti Industries Limited | Y20180001420 | I | Exact ingredient | 2022/02/14 | CDE |
| 丙酸氟替卡松 · No verified English name | Cipla Ltd | Y20180000678 | I | Exact ingredient | 2023/03/24 | CDE |
| 丙酸氟替卡松 · No verified English name | Sterling S.p.A. | Y20180000012 | A | Exact ingredient | 2026/08/30 | CDE |
| 丙酸氟替卡松 · No verified English name | Glaxo Operations UK Limited trading as Glaxo Wellcome Operations | Y20170002132 | I | Exact ingredient | — | CDE |
| 丙酸氟替卡松 · No verified English name | Hubei Heng An Fu Lin Pharma Co., Ltd. romanized | Y20170001421 | A | Exact ingredient | 2026/07/14 | CDE |
| 丙酸氟替卡松 · No verified English name | Shandong Rui Shun Pharma Co., Ltd. romanized | Y20170001404 | A | Exact ingredient | 2026/05/20 | CDE |
| 丙酸氟替卡松 · No verified English name | Wuhan Nuo An Pharma Co., Ltd. romanized | Y20170000801 | A | Exact ingredient | 2026/02/07 | CDE |
| 丙酸氟替卡松 · No verified English name | Hubei Ge Dian Ren Fu Pharma Co., Ltd. romanized | Y20170000546 | A | Exact ingredient | 2023/05/23 | CDE |
| 丙酸氟替卡松 · No verified English name | Chongqing Sheng Kai Pharmaceutical Co., Ltd. romanized | Y20170000171 | A | Exact ingredient | 2025/04/17 | CDE |
| 丙酸氟替卡松 · No verified English name | Zhejiang Xian Ju Pharmaceutical Co., Ltd. romanized | Y20170000025 | A | Exact ingredient | 2024/08/07 | 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.
CYHB2601871
Fact date: 2026/10/13 · Site observation date: 2026/10/22
View source ↗CYHB2601651
Fact date: 2026/08/28 · 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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