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Company directoryChina company filings

Duo Duo Pharma Co., Ltd. romanized

Check drug filings and source records for this company-name string.

Listed by the company name as recorded in the source, without merging affiliated entities.

Page reference 13e2d67f32

Complete CDE snapshot
2026/11/13 06:42
Matching scope
Loaded public-source records only

These counts cover loaded acceptance records only. First-applicant and co-applicant counts are not added together. CDE data as of 2026/11/13 06:42.

Drug filings

15 acceptance records as first applicant, grouped into 13 source drug names. Source data as of 2026/11/13 06:42.

Acceptance records are de-duplicated by acceptance number. Drug names are normalized only for width and whitespace; dosage forms and combinations remain separate. Application types are retained from the source. Expand a drug to inspect each record. Published drugs link to their drug pages; other names do not create new public drug pages.

Calcium Dobesilate Capsules 1 records · Latest accepted 2026/10/09

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2602461Generic2026/10/09Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ticagrelor Tablets 2 records · Latest accepted 2026/09/07

Generic · 2

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2602214Generic2026/09/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
CYHS2602213Generic2026/09/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ivabradine Hydrochloride Tablets 1 records · Latest accepted 2026/07/16

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2601695Generic2026/07/16Duo Duo Pharma Co., Ltd. romanizedCDE ↗
五加生化胶囊 · No verified English name 1 records · Latest accepted 2026/05/25

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYZB2602273Supplement2026/05/25Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Citicoline Sodium Injection 1 records · Latest accepted 2026/02/04

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHB2650042Supplement2026/02/04Duo Duo Pharma Co., Ltd. romanizedCDE ↗
金荞麦胶囊 · No verified English name 1 records · Latest accepted 2026/01/05

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYZB2600003Supplement2026/01/05Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Sitagliptin Phosphate and Metformin Hydrochloride Tablets (II) 1 records · Latest accepted 2025/10/11

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2503626Generic2025/10/11Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Bromhexine Hydrochloride Injection 1 records · Latest accepted 2025/03/20

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2501114Generic2025/03/20Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Febuxostat Tablets 2 records · Latest accepted 2024/11/07

Generic · 2

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2403807Generic2024/11/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
CYHS2403806Generic2024/11/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Tramadol Hydrochloride Injection 1 records · Latest accepted 2024/07/20

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHB2450385Supplement2024/07/20Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ambroxol Hydrochloride Injection 1 records · Latest accepted 2024/04/26

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2401261Generic2024/04/26Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Montmorillonite Powder 1 records · Latest accepted 2022/04/13

Generic · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHS2200581Generic2022/04/13Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Paracetamol and Tramadol Hydrochloride Tablets 1 records · Latest accepted 2022/03/18

Supplement · 1

Drug filings
Acceptance numberApplication typeAcceptedCompany / applicantView source
CYHB2250168Supplement2022/03/18Duo Duo Pharma Co., Ltd. romanizedCDE ↗

Changes in the last 90 days

3 events from 2026/08/16 to 2026/11/13. CDE data as of 2026/11/13 06:42; NMPA data as of 2026/11/12 18:32.

This source was last successfully updated at 2026/11/12 18:32; current coverage may be incomplete.

Last 90 days, ordered by fact date. Marketing approvals, trial registrations, supplements, notices and review changes are labelled separately. 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.

Accepted: 3 applications

  1. 2026/10/09Accepted

    Calcium Dobesilate Capsules

    CYHS2602461

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

    View source ↗
  2. 2026/09/07Accepted

    Ticagrelor Tablets

    CYHS2602214

    Fact date: 2026/09/07 · Site observation date: 2026/10/21

    View source ↗
  3. 2026/09/07Accepted

    Ticagrelor Tablets

    CYHS2602213

    Fact date: 2026/09/07 · Site observation date: 2026/10/21

    View source ↗

Under review

6 acceptance numbers with this company as first applicant are currently listed as under review by CDE. Source data as of 2026/11/13 06:42.

Under review
Drug Acceptance numberApplication typeAcceptedCompany / applicantView source
Calcium Dobesilate Capsules CYHS2602461Generic2026/10/09Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ticagrelor Tablets CYHS2602214Generic2026/09/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ticagrelor Tablets CYHS2602213Generic2026/09/07Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Ivabradine Hydrochloride Tablets CYHS2601695Generic2026/07/16Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Citicoline Sodium Injection CYHB2650042Supplement2026/02/04Duo Duo Pharma Co., Ltd. romanizedCDE ↗
Sitagliptin Phosphate and Metformin Hydrochloride Tablets (II) CYHS2503626Generic2025/10/11Duo Duo Pharma Co., Ltd. romanizedCDE ↗

Catalogue holder records

8 loaded active catalogue records whose holder name matches this source company name. Source data as of 2026/11/13 06:39. Manufacturer-only records are excluded.

DrugMarketing authorization holderManufacturerApproval numberApprovedCatalogue category (source text)View source
Bromhexine Hydrochloride InjectionDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H202659042026/09/08Generic approved under the new chemical-drug registration classificationCDE ↗
Febuxostat TabletsDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H202641932026/04/29Generic approved under the new chemical-drug registration classificationCDE ↗
Febuxostat TabletsDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H202641922026/04/29Generic approved under the new chemical-drug registration classificationCDE ↗
Tramadol Hydrochloride InjectionDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H109100362025/08/07Drug that passed quality-and-efficacy consistency evaluationCDE ↗
Ambroxol Hydrochloride InjectionDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H202550832025/08/05Generic approved under the new chemical-drug registration classificationCDE ↗
Montmorillonite PowderDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H202346512023/12/13Generic approved under the new chemical-drug registration classificationCDE ↗
Paracetamol and Tramadol Hydrochloride TabletsDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H201200402023/04/18Drug that passed quality-and-efficacy consistency evaluationCDE ↗
Tramadol Hydrochloride TabletsDuo Duo Pharma Co., Ltd. romanizedDuo Duo Pharma Co., Ltd. romanized国药准字H230207952021/07/22Drug that passed quality-and-efficacy consistency evaluationCDE ↗

Only active catalogue records matching the source holder name are listed. A manufacturer role does not count as a holder record. The catalogue covers only part of the chemical-drug market; source categories do not establish complete market coverage or qualifications.

API registrations

6 loaded active API registrations whose first registered company matches this source company name. Source data as of 2026/11/13 06:41.

NameCompany / applicantRegistration numberStatusSource update dateView source
曲克芦丁 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190007913A2025/05/22CDE ↗
胃蛋白酶 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190005311A2025/07/19CDE ↗
胃膜素 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190005305A2025/07/19CDE ↗
胰酶 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190003523A2025/05/22CDE ↗
淀粉酶 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190002295A2025/02/15CDE ↗
盐酸曲马多 · No verified English nameDuo Duo Pharma Co., Ltd. romanizedY20190001917A2025/02/15CDE ↗

Only loaded active API registrations not listed as cancelled are shown. A/I are source registration statuses. Records are listed by registration number and do not establish capacity or supply. The register does not identify the associated formulation.

Co-applicant records

0 acceptance records name this company after the first applicant. They are listed separately and are not included in first-applicant drug or filing counts. Source data as of 2026/11/13 06:42.

Co-applicant records
Drug Acceptance numberApplication typeAcceptedCompany / applicantView source
No matching records were found in the currently loaded source data; coverage dates are listed below.

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
Full API register
Last successful update: 2026/11/13 06:41
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.

Listed by the company name as recorded in the source, without merging affiliated entities.

This page summarizes loaded records only, without new source queries or collection. Parent companies, subsidiaries, former names and aliases are not merged. Counts from different sources must not be added together. No loaded record does not establish the absence of a filing or registration. Check original records where coverage is incomplete, an update has failed, or a source lies outside the loaded scope.

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.

Drugs with a verified official English name use that name only. Other drug names retain the Chinese source name marked No verified English name; names with a Chinese public page link to that page. Company labels use verified official names, Latin source names, then fixed-rule transliterations marked romanized; Chinese company names are not displayed. Marked unverified drug names and original statutory reference numbers may appear in Chinese.

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.