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Ioversol Injection(碘佛醇注射液)
Companies, stages and changes, with each record available on this page.
Last 90 days: Accepted: 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 holders10View records ↓
Under-review filings9View records ↓
This year’s generic filers2View records ↓
NHSA approval numbers26View records ↓
API companies with A status6View records ↓
Chemical-drug catalogue
Loaded records: 10 holders; 1 in the quality-and-efficacy consistency-evaluation category, and 8 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 |
|---|---|---|---|---|---|---|
| 山东齐都药业有限公司 | 博瑞制药（苏州）有限公司 | 国药准字H20264614 | 2026/06/03 | 100ml：35g（I） | 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 |
| 北京北陆药业股份有限公司 | 成都倍特药业股份有限公司 | 国药准字H20264260 | 2026/05/07 | 100ml:35g（I） | 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 |
| 重庆药友制药有限责任公司 | 重庆药友制药有限责任公司 | 国药准字H20263857 | 2026/04/07 | 50ml:16g (I) | 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 |
| 重庆药友制药有限责任公司 | 重庆药友制药有限责任公司 | 国药准字H20263858 | 2026/04/07 | 100ml:35g (I) | 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 |
| 重庆圣华曦药业股份有限公司 | 重庆圣华曦药业股份有限公司 | 国药准字H20255460 | 2025/09/09 | 100ml：32g（I） | 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 |
| 上海司太立制药有限公司 | 上海司太立制药有限公司 | 国药准字H20258146 | 2025/07/31 | 100ml:35g(I) | 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 |
| 成都倍特药业股份有限公司 | 成都倍特药业股份有限公司 | 国药准字H20249483 | 2024/12/01 | 100ml:32g(I) | 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 |
| 成都倍特药业股份有限公司 | 成都倍特药业股份有限公司 | 国药准字H20249482 | 2024/12/01 | 50ml:16g(I) | 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 |
| 成都倍特药业股份有限公司 | 成都倍特药业股份有限公司 | 国药准字H20243653 | 2024/04/30 | 100ml:35g(I) | 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 |
| 上海司太立制药有限公司 | 上海司太立制药有限公司 | 国药准字H20234353 | 2023/10/24 | 100ml:32g(I) | 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 |
| 江苏恒瑞医药股份有限公司 | 江苏恒瑞医药股份有限公司 | 国药准字H20143027 | 2023/06/08 | 100ml：35g（I） | Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) | CDE |
| 江苏恒瑞医药股份有限公司 | 江苏恒瑞医药股份有限公司 | 国药准字H20067895 | 2023/06/08 | 20ml：6.4g（I） | Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) | CDE |
| 江苏恒瑞医药股份有限公司 | 江苏恒瑞医药股份有限公司 | 国药准字H20113430 | 2023/06/08 | 100ml：32g（I） | Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) | CDE |
| 江苏恒瑞医药股份有限公司 | 江苏恒瑞医药股份有限公司 | 国药准字H20067896 | 2021/08/23 | 50ml:16g(I) | Drug that passed quality-and-efficacy consistency evaluation (通过质量和疗效一致性评价的药品) | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150571 | 1999/03/02 | 50mL:17.5g（I） | Imported originator drug (进口原研药品) | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150568 | 1999/03/02 | 100mL:32g（I） | Imported originator drug (进口原研药品) | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150572;H20150574 | 1999/03/02 | 100mL:35g（I） | Imported originator drug (进口原研药品) | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150566 | 1999/03/02 | 20mL:6.4g（I） | Imported originator drug (进口原研药品) | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150567 | 1999/03/02 | 50mL:16g（I） | Imported originator drug (进口原研药品) | CDE |
| 成都天之翼尚品医药科技有限公司 | 北京北陆药业股份有限公司 | 国药准字H20265795 | 2026/09/02 | 100ml：35g（I） | 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 | 四川汇宇制药股份有限公司 | 国药准字H20265800 | 2026/09/02 | 50ml:16g（I） | 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 | 四川汇宇制药股份有限公司 | 国药准字H20265801 | 2026/09/02 | 100ml:35g（I） | 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: 26 distinct approval numbers and 12 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| 北京北陆药业股份有限公司 | 国药准字H20264260 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010100014 | NHSA |
| 上海司太立制药有限公司 | 国药准字H20234353 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002010100621 | NHSA |
| 重庆药友制药有限责任公司 | 国药准字H20263857 | 50ml:16g (I) | Category A (甲) | XV08ABD104B002010101066 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20113430 | 100ml: 32g(I) | Category A (甲) | XV08ABD104B002010101445 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20265801 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010101606 | NHSA |
| 成都倍特药业股份有限公司 | 国药准字H20243653 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010102013 | NHSA |
| 山东齐都药业有限公司 | 国药准字H20264614 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010104145 | NHSA |
| 重庆圣华曦药业股份有限公司 | 国药准字H20255460 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002010109568 | NHSA |
| 成都天之翼尚品医药科技有限公司 | 国药准字H20265795 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010184759 | NHSA |
| 重庆煜洋药业有限公司 | 国药准字H20255433 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002010185285 | NHSA |
| 上海司太立制药有限公司 | 国药准字H20234353 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002010200621 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20265801 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002010201606 | NHSA |
| 上海司太立制药有限公司 | 国药准字H20258146 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002020100621 | NHSA |
| 重庆药友制药有限责任公司 | 国药准字H20263858 | 100ml:35g (I) | Category A (甲) | XV08ABD104B002020101066 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20143027 | 100ml: 35g(I) | Category A (甲) | XV08ABD104B002020101445 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20265800 | 50ml:16g(I) | Category A (甲) | XV08ABD104B002020101606 | NHSA |
| 成都倍特药业股份有限公司 | 国药准字H20249482 | 50ml:16g(I) | Category A (甲) | XV08ABD104B002020102013 | NHSA |
| 南京正大天晴制药有限公司 | 国药准字H20265800 | 50ml:16g(I) | Category A (甲) | XV08ABD104B002020201606 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150574 | 100mL:35g(I) | Category A (甲) | XV08ABD104B002020278927 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20067895 | 20ml:6.4g(I) | Category A (甲) | XV08ABD104B002030101445 | NHSA |
| 成都倍特药业股份有限公司 | 国药准字H20249483 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002030102013 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150570 | 125mL:40g(I) | Category A (甲) | XV08ABD104B002030178927 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20067895 | 20ml:6.4g(I) | Category A (甲) | XV08ABD104B002030201445 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20067896 | 50ml:16g(I) | Category A (甲) | XV08ABD104B002040101445 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150566 | 20mL:6.4g(I) | Category A (甲) | XV08ABD104B002040178927 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20269169 | 75ml:26.25g(I) | Category A (甲) | XV08ABD104B002050101445 | NHSA |
| 江苏恒瑞医药股份有限公司 | 国药准字H20269169 | 75ml:26.25g(I) | Category A (甲) | XV08ABD104B002050201445 | NHSA |
| GUERBET | 国药准字HJ20150567 | 50ml:16g(I) | Category A (甲) | XV08ABD104B002080178927 | NHSA |
| GUERBET | 国药准字HJ20150571 | 50ml:17.5g(I) | Category A (甲) | XV08ABD104B002080278927 | NHSA |
| GUERBET | 国药准字HJ20150568 | 100ml:32g(I) | Category A (甲) | XV08ABD104B002090178927 | NHSA |
| GUERBET | 国药准字HJ20150572 | 100ml:35g(I) | Category A (甲) | XV08ABD104B002090278927 | 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: 9 filings and 7 distinct first applicants.
Generic 7 · Supplement 2
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| 安徽佳和药业有限公司;博瑞制药（苏州）有限公司 | CYHS2502389 | Generic | 2025/07/05 | Not stated by source | CDE |
| 山东齐都药业有限公司 | CYHB2601911 | Supplement | 2026/10/19 | Not stated by source | CDE |
| 上海司太立制药有限公司 | CYHB2601803 | Supplement | 2026/09/23 | Not stated by source | CDE |
| 辰欣药业股份有限公司 | CYHS2601458 | Generic | 2026/06/18 | Not stated by source | CDE |
| 辰欣药业股份有限公司 | CYHS2601457 | Generic | 2026/06/18 | Not stated by source | CDE |
| 福建森福润医药科技有限公司;扬子江药业集团有限公司 | CYHS2600254 | Generic | 2026/01/22 | Not stated by source | CDE |
| 福建森福润医药科技有限公司;扬子江药业集团有限公司 | CYHS2504040 | Generic | 2025/11/22 | Not stated by source | CDE |
| 海南普利制药股份有限公司 | CYHS2503723 | Generic | 2025/10/17 | Not stated by source | CDE |
| 福安药业集团宁波天衡制药有限公司 | CYHS2502971 | Generic | 2025/08/14 | 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 |
|---|---|---|---|---|---|
| 辰欣药业股份有限公司 | CYHS2601458 | Generic | 2026/06/18 | Not stated by source | CDE |
| 辰欣药业股份有限公司 | CYHS2601457 | Generic | 2026/06/18 | Not stated by source | CDE |
| 福建森福润医药科技有限公司;扬子江药业集团有限公司 | CYHS2600254 | Generic | 2026/01/22 | Not stated by source | CDE |
API registrations
Non-component matches: 6 companies with A status and 2 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 |
|---|---|---|---|---|---|---|
| 碘佛醇 | 安徽普利药业有限公司 | Y20250000828 | I | Exact ingredient | 2025/08/29 | CDE |
| 碘佛醇 | 浙江海洲制药股份有限公司 | Y20250000483 | I | Exact ingredient | 2025/07/01 | CDE |
| 碘佛醇 | 江西司太立制药有限公司 | Y20240001006 | A | Exact ingredient | 2026/02/13 | CDE |
| 碘佛醇 | 重庆圣华曦药业股份有限公司 | Y20230001115 | A | Exact ingredient | 2026/02/07 | CDE |
| 碘佛醇 | 江苏宇田医药股份有限公司 | Y20220001089 | A | Exact ingredient | 2026/10/29 | CDE |
| 碘佛醇 | 江苏恒瑞医药股份有限公司 | Y20190004699 | A | Exact ingredient | 2026/07/16 | CDE |
| 碘佛醇 | 四川仁安药业有限责任公司 | Y20220000014 | A | Exact ingredient | 2025/12/12 | CDE |
| 碘佛醇 | 浙江司太立制药股份有限公司 | Y20180000462 | A | Exact ingredient | 2023/12/08 | 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.
-
2026/10/19Accepted
-
2026/09/23Accepted
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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