YaoGeJu

Public drug landscapesDrug landscape

Ioversol Injection

As 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

Follow for free
Complete CDE snapshot
2026/11/13 06:42
Matching scope
Same generic name; dosage forms and combinations kept separate

US Orange Book listing

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.

Same dosage form

Brand nameApplicant (source text)Application numberDosage 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

Other dosage forms of the same ingredient

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.

Ingredient cross-list details ↗

Which companies are listed, and at what stages?

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.

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 holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Shandong Qidu Pharmaceutical Co., Ltd.Bo Rui Pharmaceutical (Suzhou) Co., Ltd. romanized国药准字H202646142026/06/03100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE
Beijing Bei Lu Pharma Co., Ltd. romanizedChengdu Brilliant Pharmaceutical Co., Ltd.国药准字H202642602026/05/07100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE
YaoPharma Co., Ltd.YaoPharma Co., Ltd.国药准字H202638572026/04/0750ml:16g (I)Generic approved under the new chemical-drug registration classificationCDE
YaoPharma Co., Ltd.YaoPharma Co., Ltd.国药准字H202638582026/04/07100ml:35g (I)Generic approved under the new chemical-drug registration classificationCDE
Chongqing Sheng Hua Xi Pharma Co., Ltd. romanizedChongqing Sheng Hua Xi Pharma Co., Ltd. romanized国药准字H202554602025/09/09100ml:32g(I)Generic approved under the new chemical-drug registration classificationCDE
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanizedShanghai Si Tai Li Pharmaceutical Co., Ltd. romanized国药准字H202581462025/07/31100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE
Chengdu Brilliant Pharmaceutical Co., Ltd.Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H202494832024/12/01100ml:32g(I)Generic approved under the new chemical-drug registration classificationCDE
Chengdu Brilliant Pharmaceutical Co., Ltd.Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H202494822024/12/0150ml:16g(I)Generic approved under the new chemical-drug registration classificationCDE
Chengdu Brilliant Pharmaceutical Co., Ltd.Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H202436532024/04/30100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanizedShanghai Si Tai Li Pharmaceutical Co., Ltd. romanized国药准字H202343532023/10/24100ml:32g(I)Generic approved under the new chemical-drug registration classificationCDE
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H201430272023/06/08100ml:35g(I)Drug that passed quality-and-efficacy consistency evaluationCDE
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H200678952023/06/0820ml:6.4g(I)Drug that passed quality-and-efficacy consistency evaluationCDE
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H201134302023/06/08100ml:32g(I)Drug that passed quality-and-efficacy consistency evaluationCDE
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H200678962021/08/2350ml:16g(I)Drug that passed quality-and-efficacy consistency evaluationCDE
Liebel-Flarsheim Canada Inc.Liebel-Flarsheim Canada Inc.H201505711999/03/0250mL:17.5g(I)Imported originator drugCDE
Liebel-Flarsheim Canada Inc.Liebel-Flarsheim Canada Inc.H201505681999/03/02100mL:32g(I)Imported originator drugCDE
Liebel-Flarsheim Canada Inc.Liebel-Flarsheim Canada Inc.H20150572;H201505741999/03/02100mL:35g(I)Imported originator drugCDE
Liebel-Flarsheim Canada Inc.Liebel-Flarsheim Canada Inc.H201505661999/03/0220mL:6.4g(I)Imported originator drugCDE
Liebel-Flarsheim Canada Inc.Liebel-Flarsheim Canada Inc.H201505671999/03/0250mL:16g(I)Imported originator drugCDE
Chengdu Tian Zhi Yi Shang Pin Pharmaceuticals Technology Co., Ltd. romanizedBeijing Bei Lu Pharma Co., Ltd. romanized国药准字H202657952026/09/02100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.Sichuan Hui Yu Pharmaceutical Co., Ltd. romanized国药准字H202658002026/09/0250ml:16g(I)Generic approved under the new chemical-drug registration classificationCDE
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.Sichuan Hui Yu Pharmaceutical Co., Ltd. romanized国药准字H202658012026/09/02100ml:35g(I)Generic approved under the new chemical-drug registration classificationCDE

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 / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Beijing Bei Lu Pharma Co., Ltd. romanized国药准字H20264260100ml:35g(I)Category AXV08ABD104B002010100014NHSA
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized国药准字H20234353100ml:32g(I)Category AXV08ABD104B002010100621NHSA
YaoPharma Co., Ltd.国药准字H2026385750ml:16g (I)Category AXV08ABD104B002010101066NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H20113430100ml: 32g(I)Category AXV08ABD104B002010101445NHSA
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.国药准字H20265801100ml:35g(I)Category AXV08ABD104B002010101606NHSA
Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H20243653100ml:35g(I)Category AXV08ABD104B002010102013NHSA
Shandong Qidu Pharmaceutical Co., Ltd.国药准字H20264614100ml:35g(I)Category AXV08ABD104B002010104145NHSA
Chongqing Sheng Hua Xi Pharma Co., Ltd. romanized国药准字H20255460100ml:32g(I)Category AXV08ABD104B002010109568NHSA
Chengdu Tian Zhi Yi Shang Pin Pharmaceuticals Technology Co., Ltd. romanized国药准字H20265795100ml:35g(I)Category AXV08ABD104B002010184759NHSA
Chongqing Yu Yang Pharma Co., Ltd. romanized国药准字H20255433100ml:32g(I)Category AXV08ABD104B002010185285NHSA
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized国药准字H20234353100ml:32g(I)Category AXV08ABD104B002010200621NHSA
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.国药准字H20265801100ml:35g(I)Category AXV08ABD104B002010201606NHSA
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized国药准字H20258146100ml:35g(I)Category AXV08ABD104B002020100621NHSA
YaoPharma Co., Ltd.国药准字H20263858100ml:35g (I)Category AXV08ABD104B002020101066NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H20143027100ml: 35g(I)Category AXV08ABD104B002020101445NHSA
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.国药准字H2026580050ml:16g(I)Category AXV08ABD104B002020101606NHSA
Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H2024948250ml:16g(I)Category AXV08ABD104B002020102013NHSA
Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd.国药准字H2026580050ml:16g(I)Category AXV08ABD104B002020201606NHSA
Liebel-Flarsheim Canada Inc.H20150574100mL:35g(I)Category AXV08ABD104B002020278927NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H2006789520ml:6.4g(I)Category AXV08ABD104B002030101445NHSA
Chengdu Brilliant Pharmaceutical Co., Ltd.国药准字H20249483100ml:32g(I)Category AXV08ABD104B002030102013NHSA
Liebel-Flarsheim Canada Inc.H20150570125mL:40g(I)Category AXV08ABD104B002030178927NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H2006789520ml:6.4g(I)Category AXV08ABD104B002030201445NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H2006789650ml:16g(I)Category AXV08ABD104B002040101445NHSA
Liebel-Flarsheim Canada Inc.H2015056620mL:6.4g(I)Category AXV08ABD104B002040178927NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H2026916975ml:26.25g(I)Category AXV08ABD104B002050101445NHSA
Jiangsu Heng Rui Pharmaceuticals Co., Ltd. romanized国药准字H2026916975ml:26.25g(I)Category AXV08ABD104B002050201445NHSA
GUERBET国药准字HJ2015056750ml:16g(I)Category AXV08ABD104B002080178927NHSA
GUERBET国药准字HJ2015057150ml:17.5g(I)Category AXV08ABD104B002080278927NHSA
GUERBET国药准字HJ20150568100ml:32g(I)Category AXV08ABD104B002090178927NHSA
GUERBET国药准字HJ20150572100ml:35g(I)Category AXV08ABD104B002090278927NHSA

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

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Anhui Jia He Pharma Co., Ltd. romanized; Bo Rui Pharmaceutical (Suzhou) Co., Ltd. romanizedCYHS2502389Generic2025/07/05Not stated by sourceCDE
Shandong Qidu Pharmaceutical Co., Ltd.CYHB2601911Supplement2026/10/19Not stated by sourceCDE
Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanizedCYHB2601803Supplement2026/09/23Not stated by sourceCDE
CISEN PHARMACEUTICAL CO., LTD.CYHS2601458Generic2026/06/18Not stated by sourceCDE
CISEN PHARMACEUTICAL CO., LTD.CYHS2601457Generic2026/06/18Not stated by sourceCDE
Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., LtdCYHS2600254Generic2026/01/22Not stated by sourceCDE
Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., LtdCYHS2504040Generic2025/11/22Not stated by sourceCDE
Hainan Pu Li Pharmaceutical Co., Ltd. romanizedCYHS2503723Generic2025/10/17Not stated by sourceCDE
Fu An Pharma Group Ningbo Tian Heng Pharmaceutical Co., Ltd. romanizedCYHS2502971Generic2025/08/14Not stated by sourceCDE
New generic filings in 2026

Loaded records: 3 filings and 2 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
CISEN PHARMACEUTICAL CO., LTD.CYHS2601458Generic2026/06/18Not stated by sourceCDE
CISEN PHARMACEUTICAL CO., LTD.CYHS2601457Generic2026/06/18Not stated by sourceCDE
Fujian Sen Fu Run Pharmaceuticals Technology Co., Ltd. romanized; Yangtze River Pharmaceutical Group Co., LtdCYHS2600254Generic2026/01/22Not stated by sourceCDE
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.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
碘佛醇 · No verified English nameAnhui Pu Li Pharma Co., Ltd. romanizedY20250000828IExact ingredient2025/08/29CDE
碘佛醇 · No verified English nameZhejiang Hai Zhou Pharmaceutical Co., Ltd. romanizedY20250000483IExact ingredient2025/07/01CDE
碘佛醇 · No verified English nameJiangxi Si Tai Li Pharmaceutical Co., Ltd. romanizedY20240001006AExact ingredient2026/02/13CDE
碘佛醇 · No verified English nameChongqing Sheng Hua Xi Pharma Co., Ltd. romanizedY20230001115AExact ingredient2026/02/07CDE
碘佛醇 · No verified English nameJiangsu Yu Tian Pharmaceuticals Co., Ltd. romanizedY20220001089AExact ingredient2026/10/29CDE
碘佛醇 · No verified English nameJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedY20190004699AExact ingredient2026/07/16CDE
碘佛醇 · No verified English nameSichuan Ren An Pharma Co., Ltd. romanizedY20220000014AExact ingredient2025/12/12CDE
碘佛醇 · No verified English nameZhejiang Si Tai Li Pharmaceutical Co., Ltd. romanizedY20180000462AExact ingredient2023/12/08CDE

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: 2026/11/13 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.

  1. 2026/10/19Accepted

    Shandong Qidu Pharmaceutical Co., Ltd.

    CYHB2601911

    Fact date: 2026/10/19 · Site observation date: 2026/10/22

    View source ↗
  2. 2026/09/23Accepted

    Shanghai Si Tai Li Pharmaceutical Co., Ltd. romanized

    CYHB2601803

    Fact date: 2026/09/23 · Site observation date: 2026/10/22

    View source ↗

How current is each source?

CDE acceptances and review
Last successful update: 2026/11/13 06:42
Chemical-drug catalogue
Last successful update: 2026/11/13 06:39

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: 2026/11/13 06:41
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: 2026/11/12 18:32 · Current coverage may be incomplete

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.

Drug Clinical Trial Registry and Information Disclosure Platform
Last successful update: 2026/11/13 08:09 · 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: 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

Follow changes to Ioversol Injection

Up to 3 drugs per email address, in one weekly digest. Starts after email confirmation; unsubscribe at any time.

Confirmation links expire in 7 days. No digest is sent before confirmation; existing follows are not duplicated.

Sign in to choose products