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Diphenhydramine Hydrochloride Injection

As of 13 November 2026, for Diphenhydramine Hydrochloride 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 3 holders.

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

Last 90 days: No longer listed under review: 1 application

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 3 of 3 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
BENADRYL MCNEIL CONSUMER HEALTHCARE NDA 006146 · Product no. 001, 002 INJECTABLE INJECTION DISCONTINUED Approved prior to 1982 (exact date not listed)
BENADRYL PRESERVATIVE FREE MCNEIL CONSUMER HEALTHCARE NDA 009486 · Product no. 001 INJECTABLE INJECTION DISCONTINUED Approved prior to 1982 (exact date not listed)

Other dosage forms of the same ingredient

Brand nameApplicant (source text)Application numberDosage form (source text)Route (source text)Marketing status (source text)Approval date
BENADRYL MCNEIL CONSUMER HEALTHCARE NDA 005845 · Product no. 001, 007 CAPSULE ORAL DISCONTINUED Approved prior to 1982 (exact date not listed)
BENADRYL MCNEIL CONSUMER HEALTHCARE NDA 005845 · Product no. 004 ELIXIR ORAL DISCONTINUED Approved prior to 1982 (exact date not listed)
BENYLIN PARKE DAVIS DIV WARNER LAMBERT CO NDA 006514 · Product no. 004 SYRUP ORAL DISCONTINUED Approved prior to 1982 (exact date not listed)

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: 3 holders; 2 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 Zhi Tai Pharmaceuticals Technology Co., Ltd. romanizedAnhui Heng Xing Pharmaceutical Co., Ltd. romanized国药准字H202630322026/01/051ml: 50mgGeneric approved under the new chemical-drug registration classificationCDE
Sui Cheng Pharma Co., Ltd. romanizedSui Cheng Pharma Co., Ltd. romanized国药准字H202582532025/11/200.4ml:20mgDrug that passed quality-and-efficacy consistency evaluationCDE
Sui Cheng Pharma Co., Ltd. romanizedSui Cheng Pharma Co., Ltd. romanized国药准字H202582542025/11/201ml:50mgDrug that passed quality-and-efficacy consistency evaluationCDE
Shanghai Zhao Hui Pharma Co., Ltd. romanizedShanghai Zhao Hui Pharma Co., Ltd. romanized国药准字H202581392025/07/241ml:50mgDrug that passed quality-and-efficacy consistency evaluationCDE

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: 20 distinct approval numbers and 17 companies.

Company / applicantApproval numberStrength / specificationNHSA classNHSA drug codeView source
Beijing Shi Yong Kang Pharma Co., Ltd. romanized国药准字H110205231ml:20mgCategory AXR06AAB058B002010100137NHSA
Guangdong Bang Min Pharmaceutical Factory Co., Ltd. romanized国药准字H440219061ml:20mgCategory AXR06AAB058B002010100267NHSA
Guangzhou Bai Yun Shan Ming Xing Pharmaceutical Co., Ltd. romanized国药准字H440223871ml:20mgCategory AXR06AAB058B002010100375NHSA
Shanghai Zhao Hui Pharma Co., Ltd. romanized国药准字H310210871ml:20mgCategory AXR06AAB058B002010100665NHSA
Jin Yao He Ping (Tianjin) Pharmaceutical Co., Ltd. romanized国药准字H120206171ml:20mgCategory AXR06AAB058B002010100874NHSA
Xi Nan Pharma Co., Ltd. romanized国药准字H500201441ml:20mgCategory AXR06AAB058B002010100978NHSA
Ya Bang Pharmaceuticals Co., Ltd. romanized国药准字H320214351ml:20mgCategory AXR06AAB058B002010101511NHSA
Hubei Ke Lun Pharma Co., Ltd. romanized国药准字H420211751ml:20mgCategory AXR06AAB058B002010101871NHSA
Xian Li Jun Pharmaceutical Co., Ltd. romanized国药准字H610216791ml:20mgCategory AXR06AAB058B002010102503NHSA
Hebei Wan Cheng Pharmaceuticals Technology Co., Ltd. romanized国药准字H130214431ml:20mgCategory AXR06AAB058B002010102598NHSA
Topfond Pharmaceutical Co., Ltd.国药准字H410203541ml:20mgCategory AXR06AAB058B002010103098NHSA
Kai Feng Pharmaceutical (Group) Co., Ltd. romanized国药准字H410217921ml:20mgCategory AXR06AAB058B002010103139NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H410212641ml:20mgCategory AXR06AAB058B002010103204NHSA
Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized国药准字H410202251ml:20mgCategory AXR06AAB058B002010103216NHSA
Zhong Jia Bio Technology (Hubei Sheng) Co., Ltd. romanized国药准字H200539261ml:20mgCategory AXR06AAB058B002010103377NHSA
Fujian Gu Tian Pharma Co., Ltd. romanized国药准字H350201061ml:20mgCategory AXR06AAB058B002010104770NHSA
Shanghai Zhao Hui Pharma Co., Ltd. romanized国药准字H202581391ml:50mgCategory AXR06AAB058B002010106917NHSA
Shandong Zhi Tai Pharmaceuticals Technology Co., Ltd. romanized国药准字H202630321ml:50mgCategory AXR06AAB058B002010183094NHSA
Beijing Shi Yong Kang Pharma Co., Ltd. romanized国药准字H110205231ml:20mgCategory AXR06AAB058B002010200137NHSA
Guangzhou Bai Yun Shan Ming Xing Pharmaceutical Co., Ltd. romanized国药准字H440223871ml:20mgCategory AXR06AAB058B002010200375NHSA
Shanghai Zhao Hui Pharma Co., Ltd. romanized国药准字H310210871ml:20mgCategory AXR06AAB058B002010200665NHSA
Jin Yao He Ping (Tianjin) Pharmaceutical Co., Ltd. romanized国药准字H120206171ml:20mgCategory AXR06AAB058B002010200874NHSA
Xi Nan Pharma Co., Ltd. romanized国药准字H500201441ml:20mgCategory AXR06AAB058B002010200978NHSA
Ya Bang Pharmaceuticals Co., Ltd. romanized国药准字H320214351ml:20mgCategory AXR06AAB058B002010201511NHSA
Hubei Ke Lun Pharma Co., Ltd. romanized国药准字H420211751ml:20mgCategory AXR06AAB058B002010201871NHSA
Xian Li Jun Pharmaceutical Co., Ltd. romanized国药准字H610216791ml:20mgCategory AXR06AAB058B002010202503NHSA
Hebei Wan Cheng Pharmaceuticals Technology Co., Ltd. romanized国药准字H130214431ml:20mgCategory AXR06AAB058B002010202598NHSA
Topfond Pharmaceutical Co., Ltd.国药准字H410203541ml:20mgCategory AXR06AAB058B002010203098NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H410212641ml:20mgCategory AXR06AAB058B002010203204NHSA
Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanized国药准字H410202251ml:20mgCategory AXR06AAB058B002010203216NHSA
Shanghai Zhao Hui Pharma Co., Ltd. romanized国药准字H202581391ml:50mgCategory AXR06AAB058B002010206917NHSA
Shandong Zhi Tai Pharmaceuticals Technology Co., Ltd. romanized国药准字H202630321ml:50mgCategory AXR06AAB058B002010283094NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H202582530.4ml:20mgCategory AXR06AAB058B002020103204NHSA
Kai Feng Pharmaceutical (Group) Co., Ltd. romanized国药准字H410217921ml:20mgCategory AXR06AAB058B002020203139NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H202582530.4ml:20mgCategory AXR06AAB058B002020203204NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H202582541ml:50mgCategory AXR06AAB058B002030103204NHSA
Sui Cheng Pharma Co., Ltd. romanized国药准字H202582541ml:50mgCategory AXR06AAB058B002030203204NHSA

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 6 distinct first applicants.

Generic 5 · Supplement 4

Current under-review applications
Company / applicantAcceptance numberApplication typeAcceptedStrength / specificationView source
Jiangsu Run Heng Pharmaceutical Co., Ltd. romanizedCYHS2600837Generic2026/04/11Not stated by sourceCDE
Jiangsu Run Heng Pharmaceutical Co., Ltd. romanizedCYHS2600836Generic2026/04/11Not stated by sourceCDE
Anhui Wei Er Man Pharmaceutical Co., Ltd. romanizedCYHS2601497Generic2026/06/25Not stated by sourceCDE
Wuhan Bin Hu Shuang He Pharma Co., Ltd. romanized; Wuhan Fu Xing Bio Pharma Co., Ltd. romanizedCYHB2650133Supplement2026/06/10Not stated by sourceCDE
Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanizedCYHB2650036Supplement2026/01/31Not stated by sourceCDE
Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanizedCYHB2650035Supplement2026/01/31Not stated by sourceCDE
Xin Xiang Shi Chang Le Pharmaceutical Co., Ltd. romanizedCYHB2650034Supplement2026/01/31Not stated by sourceCDE
Guangzhou Rui Er Pharmaceuticals Technology Co., Ltd. romanized; E Mei Shan Tong Hui Pharmaceutical Co., Ltd. romanizedCYHS2503744Generic2025/10/21Not stated by sourceCDE
Sichuan Tian Xing Hui Pharmaceuticals Technology Co., Ltd. romanized; Chengdu Bai Yu Pharmaceutical Co., Ltd. romanizedCYHS2503453Generic2025/09/18Not 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
Jiangsu Run Heng Pharmaceutical Co., Ltd. romanizedCYHS2600837Generic2026/04/11Not stated by sourceCDE
Jiangsu Run Heng Pharmaceutical Co., Ltd. romanizedCYHS2600836Generic2026/04/11Not stated by sourceCDE
Anhui Wei Er Man Pharmaceutical Co., Ltd. romanizedCYHS2601497Generic2026/06/25Not stated by sourceCDE
API registrations

Non-component matches: 18 companies with A status and 5 I-status records. Component matches are listed separately and excluded from these counts.

NameCompany / applicantRegistration numberStatusName matchSource update dateView source
盐酸苯海拉明 · No verified English nameZhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.Y20260000429IExact ingredient2026/05/29CDE
盐酸苯海拉明 · No verified English nameLian Yun Gang Gui Ke Pharma Co., Ltd. romanizedY20250001034IExact ingredient2025/10/13CDE
盐酸苯海拉明 · No verified English nameJin Yao Pharma Co., Ltd. romanizedY20240000952IExact ingredient2024/09/09CDE
苯海拉明 · No verified English nameJin Hong Pharma Co., Ltd. romanizedY20240000477ASalt-normalized ingredient2025/09/30CDE
盐酸苯海拉明 · No verified English nameYun Peng Pharmaceuticals Group Co., Ltd. romanizedY20240000441AExact ingredient2026/01/22CDE
盐酸苯海拉明 · No verified English nameChangchun Hai Yue Pharma Co., Ltd. romanizedY20240000223AExact ingredient2026/09/29CDE
盐酸苯海拉明 · No verified English nameAnhui Heng Xing Pharmaceutical Co., Ltd. romanizedY20230001131AExact ingredient2026/11/10CDE
枸橼酸苯海拉明 · No verified English nameHefei En Rui Te Pharma Co., Ltd. romanizedY20230001060ISalt-normalized ingredient2023/11/24CDE
盐酸苯海拉明 · No verified English nameSichuan Sheng Yu Xin Pharma Co., Ltd. romanizedY20230000805AExact ingredient2026/06/27CDE
盐酸苯海拉明 · No verified English nameBai Yun Shandong Tai Shang Qiu Pharma Co., Ltd. romanizedY20230000405AExact ingredient2026/01/23CDE
盐酸苯海拉明 · No verified English nameSupriya Lifescience Ltd.Y20210001163AExact ingredient2025/09/28CDE
盐酸苯海拉明 · No verified English nameJilin Sheng Bo Da Wei Ye Pharmaceutical Co., Ltd. romanizedY20230000277AExact ingredient2024/10/29CDE
枸橼酸苯海拉明 · No verified English nameZhi En Bio Technology Co., Ltd. romanizedY20220001232ASalt-normalized ingredient2026/02/26CDE
盐酸苯海拉明 · No verified English nameAnhui Wei Er Man Pharmaceutical Co., Ltd. romanizedY20210000548AExact ingredient2023/09/15CDE
盐酸苯海拉明 · No verified English nameWanbury LimitedY20200000355AExact ingredient2026/06/13CDE
苯海拉明 · No verified English nameKongo Chemical Co., Ltd.Y20200000683ISalt-normalized ingredient2023/03/13CDE
盐酸苯海拉明 · No verified English nameShanghai Zhao Hui Pharma Co., Ltd. romanizedY20190007179AExact ingredient2023/03/24CDE
盐酸苯海拉明 · No verified English nameShanghai Shang Yao Xin Ya Pharma Co., Ltd. romanizedY20190007095AExact ingredient2023/03/24CDE
盐酸苯海拉明 · No verified English nameQi Dong Dong Yue Pharma Co., Ltd. romanizedY20190006273AExact ingredient2026/01/08CDE
盐酸苯海拉明 · No verified English nameLiao Yuan Shi Di Kang Pharma Co., Ltd. romanizedY20190005518AExact ingredient2025/05/07CDE
盐酸苯海拉明 · No verified English nameHua Run Shuang He Pharma Co., Ltd. romanizedY20190005444AExact ingredient—CDE
盐酸苯海拉明 · No verified English nameBeijing Tai Yang Pharma Co., Ltd. romanizedY20190004759AExact ingredient2025/04/23CDE
盐酸苯海拉明 · No verified English nameLiao Yuan Shi Bai Kang Pharma Co., Ltd. romanizedY20190002144AExact ingredient2025/03/22CDE

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. 2026/11/06No longer listed under review

    Anhui Chang Jiang Pharma Co., Ltd. romanized

    CYHS2501704

    Fact date: 2026/11/06 · Site observation date: 2026/11/06

    Accepted: 2025/05/10

    not on the CDE under-review list in this snapshot; the review / approval outcome is to be checked

    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.

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