Monthly
US$200
Billed every month
Sign in to subscribeAs of 13 November 2026, for Ioversol Injection, 9 applications are listed as under review at China's CDE; 2 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 10 holders.
Companies, stages and changes, with each record available on this page.
Listed in the US FDA Orange Book as OPTIRAY 320 (NDA 019710, LIEBEL-FLARSHEIM CO LLC).
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 5 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: Injection. 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.
| Brand name | Applicant (source text) | Application number | Dosage form (source text) | Route (source text) | Marketing status (source text) | Approval date |
|---|---|---|---|---|---|---|
| OPTIRAY 320 | LIEBEL-FLARSHEIM CO LLC | NDA 019710 · Product no. 001 | INJECTABLE | INJECTION | HUMAN PRESCRIPTION DRUG | 1988/12/30 |
| OPTIRAY 300 | LIEBEL-FLARSHEIM CO LLC | NDA 019710 · Product no. 004 | INJECTABLE | INJECTION | HUMAN PRESCRIPTION DRUG | 1992/01/22 |
| OPTIRAY 350 | LIEBEL-FLARSHEIM CO LLC | NDA 019710 · Product no. 005 | INJECTABLE | INJECTION | HUMAN PRESCRIPTION DRUG | 1992/01/22 |
| OPTIRAY 350 | LIEBEL-FLARSHEIM CO LLC | NDA 020923 · Product no. 003 | INJECTABLE | INJECTION | HUMAN PRESCRIPTION DRUG | 1998/05/28 |
| OPTIRAY 320 | LIEBEL-FLARSHEIM CO LLC | NDA 020923 · Product no. 002 | INJECTABLE | INJECTION | HUMAN PRESCRIPTION DRUG | 1998/05/29 |
| OPTIRAY 160 | LIEBEL-FLARSHEIM CO LLC | NDA 019710 · Product no. 003 | INJECTABLE | INJECTION | DISCONTINUED | 1988/12/30 |
| OPTIRAY 240 | LIEBEL-FLARSHEIM CO LLC | NDA 019710 · Product no. 002 | INJECTABLE | INJECTION | DISCONTINUED | 1988/12/30 |
| OPTIRAY 240 | LIEBEL-FLARSHEIM CO LLC | NDA 020923 · Product no. 001 | INJECTABLE | INJECTION | DISCONTINUED | 1998/05/28 |
| OPTIRAY 300 | LIEBEL-FLARSHEIM CO LLC | NDA 020923 · Product no. 004 | INJECTABLE | INJECTION | DISCONTINUED | 1999/05/13 |
No listings in this group among the displayed brand names.
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: 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 |
|---|---|---|---|---|---|---|
| Shandong Qidu Pharmaceutical Co., Ltd. | Bo Rui Pharmaceutical (Suzhou) Co., Ltd. romanized | 国药准字H20264614 | 2026/06/03 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Beijing Bei Lu Pharma Co., Ltd. romanized | Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20264260 | 2026/05/07 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| YaoPharma Co., Ltd. | YaoPharma Co., Ltd. | 国药准字H20263857 | 2026/04/07 | 50ml:16g (I) | Generic approved under the new chemical-drug registration classification | CDE |
| YaoPharma Co., Ltd. | YaoPharma Co., Ltd. | 国药准字H20263858 | 2026/04/07 | 100ml:35g (I) | Generic approved under the new chemical-drug registration classification | CDE |
| Chongqing Sheng Hua Xi Pharma Co., Ltd. romanized | Chongqing Sheng Hua Xi Pharma Co., Ltd. romanized | 国药准字H20255460 | 2025/09/09 | 100ml:32g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | 国药准字H20258146 | 2025/07/31 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20249483 | 2024/12/01 | 100ml:32g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20249482 | 2024/12/01 | 50ml:16g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20243653 | 2024/04/30 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | 国药准字H20234353 | 2023/10/24 | 100ml:32g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20143027 | 2023/06/08 | 100ml:35g(I) | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20067895 | 2023/06/08 | 20ml:6.4g(I) | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20113430 | 2023/06/08 | 100ml:32g(I) | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20067896 | 2021/08/23 | 50ml:16g(I) | Drug that passed quality-and-efficacy consistency evaluation | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150571 | 1999/03/02 | 50mL:17.5g(I) | Imported originator drug | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150568 | 1999/03/02 | 100mL:32g(I) | Imported originator drug | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150572;H20150574 | 1999/03/02 | 100mL:35g(I) | Imported originator drug | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150566 | 1999/03/02 | 20mL:6.4g(I) | Imported originator drug | CDE |
| Liebel-Flarsheim Canada Inc. | Liebel-Flarsheim Canada Inc. | H20150567 | 1999/03/02 | 50mL:16g(I) | Imported originator drug | CDE |
| Chengdu Tian Zhi Yi Shang Pin Pharmaceuticals Technology Co., Ltd. romanized | Beijing Bei Lu Pharma Co., Ltd. romanized | 国药准字H20265795 | 2026/09/02 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | Sichuan Hui Yu Pharmaceutical Co., Ltd. romanized | 国药准字H20265800 | 2026/09/02 | 50ml:16g(I) | Generic approved under the new chemical-drug registration classification | CDE |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | Sichuan Hui Yu Pharmaceutical Co., Ltd. romanized | 国药准字H20265801 | 2026/09/02 | 100ml:35g(I) | Generic approved under the new chemical-drug registration classification | 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.
Loaded records: 26 distinct approval numbers and 12 companies.
| Company / applicant | Approval number | Strength / specification | NHSA class | NHSA drug code | View source |
|---|---|---|---|---|---|
| Beijing Bei Lu Pharma Co., Ltd. romanized | 国药准字H20264260 | 100ml:35g(I) | Category A | XV08ABD104B002010100014 | NHSA |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | 国药准字H20234353 | 100ml:32g(I) | Category A | XV08ABD104B002010100621 | NHSA |
| YaoPharma Co., Ltd. | 国药准字H20263857 | 50ml:16g (I) | Category A | XV08ABD104B002010101066 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20113430 | 100ml: 32g(I) | Category A | XV08ABD104B002010101445 | NHSA |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | 国药准字H20265801 | 100ml:35g(I) | Category A | XV08ABD104B002010101606 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20243653 | 100ml:35g(I) | Category A | XV08ABD104B002010102013 | NHSA |
| Shandong Qidu Pharmaceutical Co., Ltd. | 国药准字H20264614 | 100ml:35g(I) | Category A | XV08ABD104B002010104145 | NHSA |
| Chongqing Sheng Hua Xi Pharma Co., Ltd. romanized | 国药准字H20255460 | 100ml:32g(I) | Category A | XV08ABD104B002010109568 | NHSA |
| Chengdu Tian Zhi Yi Shang Pin Pharmaceuticals Technology Co., Ltd. romanized | 国药准字H20265795 | 100ml:35g(I) | Category A | XV08ABD104B002010184759 | NHSA |
| Chongqing Yu Yang Pharma Co., Ltd. romanized | 国药准字H20255433 | 100ml:32g(I) | Category A | XV08ABD104B002010185285 | NHSA |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | 国药准字H20234353 | 100ml:32g(I) | Category A | XV08ABD104B002010200621 | NHSA |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | 国药准字H20265801 | 100ml:35g(I) | Category A | XV08ABD104B002010201606 | NHSA |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | 国药准字H20258146 | 100ml:35g(I) | Category A | XV08ABD104B002020100621 | NHSA |
| YaoPharma Co., Ltd. | 国药准字H20263858 | 100ml:35g (I) | Category A | XV08ABD104B002020101066 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20143027 | 100ml: 35g(I) | Category A | XV08ABD104B002020101445 | NHSA |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | 国药准字H20265800 | 50ml:16g(I) | Category A | XV08ABD104B002020101606 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20249482 | 50ml:16g(I) | Category A | XV08ABD104B002020102013 | NHSA |
| Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd. | 国药准字H20265800 | 50ml:16g(I) | Category A | XV08ABD104B002020201606 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150574 | 100mL:35g(I) | Category A | XV08ABD104B002020278927 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20067895 | 20ml:6.4g(I) | Category A | XV08ABD104B002030101445 | NHSA |
| Chengdu Brilliant Pharmaceutical Co., Ltd. | 国药准字H20249483 | 100ml:32g(I) | Category A | XV08ABD104B002030102013 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150570 | 125mL:40g(I) | Category A | XV08ABD104B002030178927 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20067895 | 20ml:6.4g(I) | Category A | XV08ABD104B002030201445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20067896 | 50ml:16g(I) | Category A | XV08ABD104B002040101445 | NHSA |
| Liebel-Flarsheim Canada Inc. | H20150566 | 20mL:6.4g(I) | Category A | XV08ABD104B002040178927 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20269169 | 75ml:26.25g(I) | Category A | XV08ABD104B002050101445 | NHSA |
| Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | 国药准字H20269169 | 75ml:26.25g(I) | Category A | XV08ABD104B002050201445 | NHSA |
| GUERBET | 国药准字HJ20150567 | 50ml:16g(I) | Category A | XV08ABD104B002080178927 | NHSA |
| GUERBET | 国药准字HJ20150571 | 50ml:17.5g(I) | Category A | XV08ABD104B002080278927 | NHSA |
| GUERBET | 国药准字HJ20150568 | 100ml:32g(I) | Category A | XV08ABD104B002090178927 | NHSA |
| GUERBET | 国药准字HJ20150572 | 100ml:35g(I) | Category A | 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.
Loaded records: 9 filings and 7 distinct first applicants.
Generic 7 · Supplement 2
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| Anhui Jia He Pharma Co., Ltd. romanized; Bo Rui Pharmaceutical (Suzhou) Co., Ltd. romanized | CYHS2502389 | Generic | 2025/07/05 | Not stated by source | CDE |
| Shandong Qidu Pharmaceutical Co., Ltd. | CYHB2601911 | Supplement | 2026/10/19 | Not stated by source | CDE |
| Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized | CYHB2601803 | Supplement | 2026/09/23 | Not stated by source | CDE |
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2601458 | Generic | 2026/06/18 | Not stated by source | CDE |
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2601457 | Generic | 2026/06/18 | Not stated by source | CDE |
| Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., Ltd | CYHS2600254 | Generic | 2026/01/22 | Not stated by source | CDE |
| Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., Ltd | CYHS2504040 | Generic | 2025/11/22 | Not stated by source | CDE |
| Hainan Pu Li Pharmaceutical Co., Ltd. romanized | CYHS2503723 | Generic | 2025/10/17 | Not stated by source | CDE |
| Fu An Pharma Group Ningbo Tian Heng Pharmaceutical Co., Ltd. romanized | CYHS2502971 | Generic | 2025/08/14 | Not stated by source | CDE |
Loaded records: 3 filings and 2 distinct first applicants.
| Company / applicant | Acceptance number | Application type | Accepted | Strength / specification | View source |
|---|---|---|---|---|---|
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2601458 | Generic | 2026/06/18 | Not stated by source | CDE |
| CISEN PHARMACEUTICAL CO., LTD. | CYHS2601457 | Generic | 2026/06/18 | Not stated by source | CDE |
| Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., Ltd | CYHS2600254 | Generic | 2026/01/22 | Not stated by source | CDE |
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 · No verified English name | Anhui Pu Li Pharma Co., Ltd. romanized | Y20250000828 | I | Exact ingredient | 2025/08/29 | CDE |
| 碘佛醇 · No verified English name | Zhejiang Hai Zhou Pharmaceutical Co., Ltd. romanized | Y20250000483 | I | Exact ingredient | 2025/07/01 | CDE |
| 碘佛醇 · No verified English name | Jiangxi Si Tai Li Pharmaceutical Co., Ltd. romanized | Y20240001006 | A | Exact ingredient | 2026/02/13 | CDE |
| 碘佛醇 · No verified English name | Chongqing Sheng Hua Xi Pharma Co., Ltd. romanized | Y20230001115 | A | Exact ingredient | 2026/02/07 | CDE |
| 碘佛醇 · No verified English name | Jiangsu Yu Tian Pharmaceuticals Co., Ltd. romanized | Y20220001089 | A | Exact ingredient | 2026/10/29 | CDE |
| 碘佛醇 · No verified English name | Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized | Y20190004699 | A | Exact ingredient | 2026/07/16 | CDE |
| 碘佛醇 · No verified English name | Sichuan Ren An Pharma Co., Ltd. romanized | Y20220000014 | A | Exact ingredient | 2025/12/12 | CDE |
| 碘佛醇 · No verified English name | Zhejiang Si Tai Li Pharmaceutical Co., Ltd. romanized | 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.
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.
CYHB2601911
Fact date: 2026/10/19 · Site observation date: 2026/10/22
View source ↗CYHB2601803
Fact date: 2026/09/23 · 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.
Free follow
Up to 3 drugs per email address, in one weekly digest. Starts after email confirmation; unsubscribe at any time.
Subscriptions
US$200
Billed every month
Sign in to subscribeUS$540
Billed every three months
US$180 per month
Sign in to subscribeUS$1,920
Billed every year
US$160 per month
Sign in to subscribeSeparate one-time purchase
Full table and CSV export for 12 months from payment, with monthly data updates. No automatic renewal.
Subscriptions and comparison-table access are purchased separately. Neither includes the other.
Billed by Creem, our merchant of record · Terms · Refund policy