Marketing-authorisation holder · India
Sun Pharmaceutical Industries Limited
8 medicines in 2 countries, as authorisation holder and manufacturer.
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Marketing-authorisation holder · India
8 medicines in 2 countries, as authorisation holder and manufacturer.
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Every medicine in the registers under its name, current ones first.
8 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| CAVERTA 100MG F.C.TABLET | Sildenafil | Saudi Arabia | Authorised | |
| CAVERTA 50 MG F.C.TABLET | Sildenafil | Saudi Arabia | Authorised | |
| ROSUVAS 10 MG FILM COATED TABLET | Rosuvastatin | Saudi Arabia | Authorised | |
| ROSUVAS 20 MG FILM COATED TABLET | Rosuvastatin | Saudi Arabia | Authorised | |
| STORVAS 10MG F.C.TABLET | Atorvastatin | Saudi Arabia | Authorised | |
| STORVAS 20MG F.C.TABLET | Atorvastatin | Saudi Arabia | Authorised | |
| STORVAS 40MG F.C.TABLET | Atorvastatin | Saudi Arabia | Authorised | |
| POMALIDOMIDE1mg | 2mg | 3mg | 4mg · Capsule | Pomalidomide | United States | tentative | 2026 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| Saudi Arabia | 7 | 7 | 0 | CompaniesAll medicines |
| United States | 1 | 0 | 1 | CompaniesAll medicines |
The active substances in most of its medicines.
How the registers spell it, normalised: legal forms, accents and capitals removed.
Compiled by Prognia from the public medicine and company registers below. Logos are not used.
Source: U.S. FDA, Drugs@FDA / openFDA. FDA does not endorse this site.
Licence: Public domain (U.S. Government work)
Anvisa, official medicine/API manufacturer factual export, HTTP source version Fri, 09 Oct 2026 08:21:54 GMT, acquired 2026-10-09; exact unmodified native identifiers and fields preserved.
Licence: Brazil federal factual open-data reuse; Decreto 8777/2016 consolidated article 4 and third-party exceptions
Health Canada, Drug Product Database, company API, entire response observed 2026-10-10T15:12:05.508784+00:00; native facts projected by Prognia.
Licence: Open Government Licence Canada
Health Canada, Drug Product Database, drugproduct API, entire response observed 2026-10-10T15:12:07.336870+00:00; native facts projected by Prognia.
Licence: Open Government Licence Canada
GLEIF; exact source URLs/locators, version status and retrieval dates. Normalized by Prognia; no official endorsement.
Licence: CC0
Saudi Food and Drug Authority (SFDA), foreign human medicine open-data listing, source scope 2023, retrieved 11 October 2026 UTC; exact original file and response modification date retained.
Licence: Exact SFDA open-data section explicitly offers freely usable named human medicine workbooks; factual-data scope only
Contains information from HSA Listing of Registered Therapeutic Products accessed on 8 October 2026 from data.gov.sg, under Singapore Open Data Licence 1.0: https://data.gov.sg/open-data-licence
Licence: Singapore Open Data Licence
FDA Purple Book, September 2026 release; acquired 2026-10-10T15:29:54.330165+00:00; exact source fields retained with source-key projections.
Licence: FDA-created structured factual administrative metadata; public-domain policy with third-party exceptions
Report an error or request removalCorrections from the company itself are welcome.
Other companies in the same group.