ABBOTT LABORATORIES LIMITED
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 2b88da9cfc
These counts cover loaded acceptance records only. First-applicant and co-applicant counts are not added together. CDE data as of 2026/11/11 06:42.
Drug filings
16 acceptance records as first applicant, grouped into 4 source drug names. Source data as of 2026/11/11 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.
Choline Fenofibrate Sustained-release Capsules 3 records · Latest accepted 2026/11/06
Supplement · 2Import re-registration · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| JYHB2600601 | Supplement | 2026/11/06 | ABBOTT LABORATORIES LIMITED; FOURNIER LABORATORIES IRELAND LIMITED | CDE ↗ |
| JYHZ2500211 | Import re-registration | 2025/09/28 | ABBOTT LABORATORIES LIMITED; FOURNIER LABORATORIES IRELAND LIMITED; Shanghai Abbott Pharmaceutical Co. Ltd. | CDE ↗ |
| JYHB2500278 | Supplement | 2025/05/21 | ABBOTT LABORATORIES LIMITED; FOURNIER LABORATORIES IRELAND LIMITED | CDE ↗ |
Omega-3-acid ethyl ester 90 Soft Capsules 2 records · Latest accepted 2026/09/16
Import re-registration · 1Supplement · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| JYHZ2600223 | Import re-registration | 2026/09/16 | ABBOTT LABORATORIES LIMITED; PATHEON SOFTGELS B.V.; Shanghai Abbott Pharmaceutical Co. Ltd. | CDE ↗ |
| JYHB2500307 | Supplement | 2025/06/07 | ABBOTT LABORATORIES LIMITED; PATHEON SOFTGELS B. V. | CDE ↗ |
Pinaverium Bromide Tablets 1 records · Latest accepted 2025/08/16
Import re-registration · 1
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| JYHZ2500186 | Import re-registration | 2025/08/16 | ABBOTT LABORATORIES LIMITED; MYLAN LABORATORIES SAS; Shanghai Abbott Pharmaceutical Co. Ltd. | CDE ↗ |
Fenofibrate Capsules 10 records · Latest accepted 2024/08/09
Supplement · 8Import re-registration · 2
| Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|
| JYHB2400436 | Supplement | 2024/08/09 | ABBOTT LABORATORIES LIMITED; Astrea Fontaine | CDE ↗ |
| JYHB2400435 | Supplement | 2024/08/09 | ABBOTT LABORATORIES LIMITED; Astrea Fontaine | CDE ↗ |
| JYHB2300318 | Supplement | 2023/05/30 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
| JYHB2300317 | Supplement | 2023/05/30 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
| JYHZ2200131 | Import re-registration | 2022/05/27 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE; ABBOTT LABORATORIES TRADING (SHANGHAI) CO. LTD. | CDE ↗ |
| JYHZ2200130 | Import re-registration | 2022/05/27 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE; ABBOTT LABORATORIES TRADING (SHANGHAI) CO. LTD. | CDE ↗ |
| JYHB2101535 | Supplement | 2021/11/17 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
| JYHB2101534 | Supplement | 2021/11/17 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
| JYHB2101465 | Supplement | 2021/10/21 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
| JYHB2101464 | Supplement | 2021/10/21 | ABBOTT LABORATORIES LIMITED; RECIPHARM FONTAINE | CDE ↗ |
Changes in the last 90 days
2 events from 2026/08/14 to 2026/11/11. CDE data as of 2026/11/11 06:42; NMPA data as of 2026/11/10 18:31.
This source was last successfully updated at 2026/11/10 18:31; 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: 2 applications
- 2026/11/06Accepted
Choline Fenofibrate Sustained-release Capsules
JYHB2600601
Fact date: 2026/11/06 · Site observation date: 2026/11/07
View source ↗ - 2026/09/16Accepted
Omega-3-acid ethyl ester 90 Soft Capsules
JYHZ2600223
Fact date: 2026/09/16 · Site observation date: 2026/10/22
View source ↗
Under review
2 acceptance numbers with this company as first applicant are currently listed as under review by CDE. Source data as of 2026/11/11 06:42.
| Drug | Acceptance number | Application type | Accepted | Company / applicant | View source |
|---|---|---|---|---|---|
| Choline Fenofibrate Sustained-release Capsules | JYHB2600601 | Supplement | 2026/11/06 | ABBOTT LABORATORIES LIMITED; FOURNIER LABORATORIES IRELAND LIMITED | CDE ↗ |
| Omega-3-acid ethyl ester 90 Soft Capsules | JYHZ2600223 | Import re-registration | 2026/09/16 | ABBOTT LABORATORIES LIMITED; PATHEON SOFTGELS B.V.; Shanghai Abbott Pharmaceutical Co. Ltd. | CDE ↗ |
Catalogue holder records
1 loaded active catalogue records whose holder name matches this source company name. Source data as of 2026/11/11 06:38. Manufacturer-only records are excluded.
| Drug | Marketing authorization holder | Manufacturer | Approval number | Approved | Catalogue category (source text) | View source |
|---|---|---|---|---|---|---|
| Fenofibrate Capsules | ABBOTT LABORATORIES LIMITED | RECIPHARM FONTAINE | H20181240;H20181239 | 1992/06/15 | Imported originator drug | CDE ↗ |
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
0 loaded active API registrations whose first registered company matches this source company name. Source data as of 2026/11/11 06:40.
| Name | Company / applicant | Registration number | Status | Source update date | View source |
|---|---|---|---|---|---|
| No matching records were found in the currently loaded source data; coverage dates are listed below. | |||||
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 2026/11/11 06:42.
| Drug | Acceptance number | Application type | Accepted | Company / applicant | View 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: 2026/11/11 06:42
- Chemical-drug catalogue
- Last successful update: 2026/11/11 06:38
- Full API register
- Last successful update: 2026/11/11 06:40
- NMPA drug delivery notices
- Last successful update: 2026/11/10 18:31 · Current coverage may be incomplete
First index-page publication dates: — to —; 0 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.
Drug names use verified official English names only. Missing names are shown as No verified English name, linking to a Chinese page. Company labels use verified official names, Latin source names, then fixed-rule transliterations marked romanized. Original statutory reference numbers are the sole visible Chinese exception.
Legal reference identifiers are retained verbatim. Company labels use official English entries where available, or a visibly marked fixed romanization. Chinese free text is not displayed; use the source links or source-name columns in CSV exports.