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Cetirizine Hydrochloride Injection

As of 13 November 2026, for Cetirizine Hydrochloride Injection, 2 applications are listed as under review at China's CDE; 2 companies have filed new generic applications in 2026; the chemical-drug catalogue lists 1 holder.

Companies, stages and changes, with each record available on this page.

Last 90 days: Accepted: 1 application

Current coverage may be incomplete

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

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: 1 holders; 0 in the quality-and-efficacy consistency-evaluation category, and 1 in the new chemical-registration-classification generic category. Category counts may overlap.

Marketing authorization holderManufacturerApproval numberApprovedStrength / specificationCatalogue category (source text)View source
Shandong Ke Xin Hui Yi Pharma Co., Ltd. romanizedChengdu Bai Yu Pharmaceutical Co., Ltd. romanized国药准字H202442992024/06/281ml:10mgGeneric 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: 1 distinct approval numbers and 1 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Shandong Ke Xin Hui Yi Pharma Co., Ltd. romanized国药准字H202442991ml:10mgNot stated by sourceXR06AEX017B002010184618NHSA
Shandong Ke Xin Hui Yi Pharma Co., Ltd. romanized国药准字H202442991ml:10mgNot stated by sourceXR06AEX017B002010284618NHSA
Shandong Ke Xin Hui Yi Pharma Co., Ltd. romanized国药准字H202442991ml:10mgNot stated by sourceXR06AEX017B002010384618NHSA

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: 2 filings and 2 distinct first applicants.

Generic 2

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Haerbin Yu Heng Pharmaceutical Co., Ltd. romanizedCYHS2602030Generic2026/08/17Not stated by sourceCDE
Shandong Xin Shi Dai Pharma Co., Ltd. romanizedCYHS2601399Generic2026/06/12Not stated by sourceCDE
New generic filings in 2026

Loaded records: 2 filings and 2 distinct first applicants.

New generic filings in 2026
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Shandong Bai Nuo Pharmaceuticals Co., Ltd. romanized; Haerbin Yu Heng Pharmaceutical Co., Ltd. romanizedCYHS2602030Generic2026/08/17Not stated by sourceCDE
Shandong Xin Shi Dai Pharma Co., Ltd. romanizedCYHS2601399Generic2026/06/12Not stated by sourceCDE
API registrations

Non-component matches: 20 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
盐酸西替利嗪 · No verified English nameZhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.Y20260000664IExact ingredient2026/07/29CDE
盐酸西替利嗪 · No verified English nameCOSMA S.P.AY20220001058AExact ingredient2024/08/14CDE
盐酸西替利嗪 · No verified English nameGLOCHEM INDUSTRIES PRIVATE LIMITEDY20220000655AExact ingredient2026/08/20CDE
盐酸西替利嗪 · No verified English namePRAVEEN LABORATORIES PVT LTDY20210000807AExact ingredient2024/06/27CDE
盐酸西替利嗪 · No verified English nameHunan Xiang Yi Kang Pharmaceutical Co., Ltd. romanizedY20200001518AExact ingredient2025/09/02CDE
盐酸西替利嗪 · No verified English nameHunan Hua Na Da Pharmaceutical Factory Shou Xing Drug Co., Ltd. romanizedY20200000310AExact ingredient2023/03/24CDE
盐酸西替利嗪 · No verified English nameGranules India LimitedY20190009950AExact ingredient2026/10/22CDE
盐酸西替利嗪 · No verified English nameYang Zi Jiang Pharma Group Jiangsu Hai Ci Bio Pharma Co., Ltd. romanizedY20190009497AExact ingredient2025/03/27CDE
盐酸西替利嗪 · No verified English nameZhejiang Zhe Bei Pharma Co., Ltd. romanizedY20190007487AExact ingredient2024/02/05CDE
盐酸西替利嗪 · No verified English nameNanjing Sheng He Pharma Co., Ltd. romanizedY20190006224AExact ingredient2025/12/24CDE
盐酸西替利嗪 · No verified English nameYi Bin Hong Guang Pharmaceutical Factory romanizedY20190005694AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameChangzhou Si Yao Pharmaceutical Co., Ltd. romanizedY20190004909AExact ingredient2026/04/20CDE
盐酸西替利嗪 · No verified English nameZhejiang Hua Na Pharma Co., Ltd. romanizedY20190004511AExact ingredient2024/03/01CDE
盐酸西替利嗪 · No verified English nameJiangsu Lianhuan Pharmaceutical Co.,Ltd.Y20190004258AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameKun Shan Long Deng Rui Di Pharmaceutical Co., Ltd. romanizedY20190004109AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameSuzhou Dong Rui Pharmaceutical Co., Ltd. romanizedY20190004086AExact ingredient2025/07/24CDE
盐酸西替利嗪 · No verified English nameJiangsu Heng Rui Pharmaceuticals Co., Ltd. romanizedY20190004020AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameChongqing Xi Nan He Cheng Pharmaceutical Co., Ltd. romanizedY20190003311AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameLu Nan Bei Te Pharmaceutical Co., Ltd. romanizedY20190002178AExact ingredient2025/01/21CDE
盐酸西替利嗪 · No verified English nameChengdu Ao Bang Pharma Co., Ltd. romanizedY20190002122AExact ingredient2026/02/05CDE
盐酸西替利嗪 · No verified English nameQilu Pharmaceutical Co., Ltd.Y20190001565AExact ingredient—CDE
盐酸西替利嗪 · No verified English nameYang Zi Jiang Pharma Group Jiangsu Hai Ci Bio Pharma Co., Ltd. romanizedY20190000882IExact ingredient2019/10/25CDE

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. 2026/08/17Accepted

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.

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