Hainan Ai Ke Pharmaceutical Co., Ltd. romanized

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.

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.

Marketing application approved: 3 applicationsNo longer listed under review: 5 applicationsSupplement delivery: 1 application

1. 2026/11/04No longer listed under review

   腹膜透析液(乳酸盐-G1.5%) · No verified English name

   CYHS2401754

   Fact date: 2026/11/04 · Site observation date: 2026/11/04

   Accepted: 2024/06/12

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

   View source ↗
2. 2026/11/04No longer listed under review

   腹膜透析液(乳酸盐-G2.5%) · No verified English name

   CYHS2401751

   Fact date: 2026/11/04 · Site observation date: 2026/11/04

   Accepted: 2024/06/12

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

   View source ↗
3. 2026/11/04No longer listed under review

   低钙腹膜透析液(乳酸盐-G2.5%) · No verified English name

   CYHS2401749

   Fact date: 2026/11/04 · Site observation date: 2026/11/04

   Accepted: 2024/06/12

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

   View source ↗
4. 2026/11/04No longer listed under review

   低钙腹膜透析液(乳酸盐-G1.5%) · No verified English name

   CYHS2401741

   Fact date: 2026/11/04 · Site observation date: 2026/11/04

   Accepted: 2024/06/11

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

   View source ↗
5. 2026/11/03Supplement delivery

   盐酸尼卡地平氯化钠注射液 · No verified English name

   CYHB2601500 · 国药准字H20266501

   Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

   Supplemental application; excluded from new marketing approvals.

   View source · Table row 6 ↗
6. 2026/11/03Marketing application approved

   生理氯化钠溶液 · No verified English name

   CYHS2500484 · 国药准字H20266426

   Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

   View source · Table row 22 ↗
7. 2026/11/03Marketing application approved

   生理氯化钠溶液 · No verified English name

   CYHS2500483 · 国药准字H20266425

   Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

   View source · Table row 21 ↗
8. 2026/11/03Marketing application approved

   盐酸尼卡地平氯化钠注射液 · No verified English name

   CYHS2402794 · 国药准字H20266501

   Fact date: 2026/11/03 · Publication date: 2026/11/05 · Site observation date: 2026/11/06

   View source · Table row 6 ↗
9. 2026/10/29No longer listed under review

   盐酸尼卡地平氯化钠注射液 · No verified English name

   CYHB2601500

   Fact date: 2026/10/29 · Site observation date: 2026/10/29

   Accepted: 2026/08/05

   not on the CDE under-review list in this snapshot; NMPA published approval-document delivery for this acceptance number on 2026/11/05 (approval no.: 国药准字H20266501; approval date: 2026/11/03); this is a supplemental application, not counted as a new marketing approval · NMPA source · row 6

   NMPA · Table row 6 ↗ View source ↗

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.

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.

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.

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.

Public drug landscapes ↗