Where it is registered
Each register with its number of medicines and a few of them.
All medicines with Omeprazole n/a
Every register, a page at a time. Strengths and packs are on each medicine’s page.
13 results
| Medicine | Register | Strength | Form | Status | Holder |
|---|---|---|---|---|---|
| Omeprazole | United States | 20MG | tablet, delayed release | Marketed | Apotex |
| Omeprazole | United States | 20MG | tablet, orally disintegrating, delayed release | Marketed | Dexcel |
| Omeprazole | United States | 10MG, 20MG, 40MG | capsule, delayed rel pellets | Marketed | Xiromed |
| Omeclamox-PakCombination | United States | 500MG,N/A,N/A; 500MG,N/A; 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | capsule, tablet, capsule, delayed release | Not marketed | Cumberland |
| Omeprazole and Sodium BicarbonateCombination | United States | 20MG/PACKET; 1.68GM/PACKET, 40MG/PACKET; 1.68GM/PACKET | for suspension | Marketed | Novitium Pharma |
| KonvomepCombination | United States | 2MG/ML; 84MG/ML | for suspension | Marketed | Azurity |
| Prilosec OTC | United States | 20MG BASE | tablet, delayed release | Marketed | Astrazeneca |
| TaliciaCombination | United States | 250MG; 10MG BASE; 12.5MG | capsule, delayed release | Marketed | Talicia Holdings |
| Magnesium Hydroxide and Omeprazole and Sodium BicarbonateCombination | United States | 343MG; 20MG; 750MG, 343MG; 40MG; 750MG | tablet | Not marketed | Santarus |
| Prilosec | United States | 10MG BASE/PACKET, 2.5MG BASE/PACKET | for suspension, delayed release | Marketed | Azurity |
| Aspirin; OmeprazoleCombination | United States | 325MG; 40MG, 81MG; 40MG | tablet | Tentative approval | Teva Pharms USA INC |
| YospralaCombination | United States | 325MG; 40MG, 81MG; 40MG | tablet, delayed release | Not marketed | Genus Lifesciences |
| Prilosec | United States | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | capsule, delayed rel pellets | Not marketed | Astrazeneca |
Brand names
The same brand on several registers.
Companies
The companies holding its medicines, the most first.
Often combined with
Substances it shares a medicine with.
Sources
Compiled by Prognia from the public medicine registers of FDA. Each medicine’s page names its own source, licence and attribution.
Report an error or request removalCorrections from a register or a company are welcome.
For reference and learning, not treatment advice. Always check the official product information.
At a glance
- Registers
- 1
- Medicines
- 1
- Companies
- 1



