Marketing-authorisation holder
Bayer Schering Pharma AG
15 medicines in 2 countries, as authorisation holder and manufacturer.
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Marketing-authorisation holder
15 medicines in 2 countries, as authorisation holder and manufacturer.
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Every medicine in the registers under its name, current ones first.
15 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| AZAMUN | Azathioprine | Saudi Arabia | Authorised | |
| CARBOMIX 50GM POWDER | Charcoal | Saudi Arabia | Authorised | |
| LEVITRA 10 mg orodispersible tablet | Vardenafil | Saudi Arabia | Authorised | |
| OFTAN TIMOLOL 0.25% EYE DROPS | Timolol | Saudi Arabia | Authorised | |
| OFTAN TIMOLOL 0.25% EYE DROPS | Timolol | Saudi Arabia | Authorised | |
| OFTAN TIMOLOL 0.5% EYE DROPS | Timolol | Saudi Arabia | Authorised | |
| OFTAN TIMOLOL 0.5% EYE DROPS | Timolol | Saudi Arabia | Authorised | |
| OFTANEX 0.1% EYE DROPS | Dipivefrine | Saudi Arabia | Authorised | |
| PRIMOGONYL 1000 I.U AMP | Gonadotrophin chorionic human | Saudi Arabia | Authorised | |
| PRIMOGONYL 5000-1.U. AMP | Gonadotrophin chorionic human | Saudi Arabia | Authorised | |
| SALBUVENT 2MG TAB | Salbutamol | Saudi Arabia | Authorised | |
| SALBUVENT 4MG TAB | Salbutamol | Saudi Arabia | Authorised | |
| SALBUVENT INHALATION 100MCG-DOSE | Salbutamol | Saudi Arabia | Authorised | |
| TAMOFEN 20MG TAB | Tamoxifen | Saudi Arabia | Authorised | |
| Recothrom | Thrombin | EU (EMA) | Refused |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| Saudi Arabia | 14 | 14 | 0 | CompaniesAll medicines |
| European Union (EMA) | 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: European Medicines Agency (EPAR data).
Licence: EMA reuse policy (source acknowledgement required)
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
Report an error or request removalCorrections from the company itself are welcome.
Other companies in the same group.