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Each register with its number of medicines and a few of them.
Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.
AEMPS · 33 medicines
FDA · 14 medicines
AIFA · 13 medicines
SFDA · 13 medicines · Historical list
CBG-MEB · 9 medicines
HSA · 6 medicines
MS · 5 medicines · Historical list
PHARMAC · 2 medicines
ALIMS · 2 medicines
EMA · 1 medicine · Historical list
Show all 1HALMED · 1 medicine
Every register, a page at a time. Strengths and packs are on each medicine’s page.
14 results
| Medicine | Register | Strength | Form | Status | Holder |
|---|---|---|---|---|---|
| Fluoxetine | United States | 10MG BASE, 20MG BASE | capsule | Not marketed | Sun Pharm Industries |
| Fluoxetine Hydrochloride | United States | 10MG BASE, 20MG BASE, 40MG BASE … | tablet | Marketed | PH Health |
| Fluoxetine Hydrochloride | United States | 10MG BASE, 20MG BASE, 40MG BASE | capsule | Marketed | Carlsbad |
| Fluoxetine Hydrochloride | United States | 20MG BASE/5ML | solution | Marketed | Aurobindo Pharma |
| Fluoxetine Hydrochloride | United States | 90MG BASE | capsule, delayed rel pellets | Marketed | DR Reddys Labs LTD |
| Olanzapine and Fluoxetine HydrochlorideCombination | United States | 25MG BASE; 12MG BASE, 25MG BASE; 3MG BASE, 25MG BASE; 6MG BASE … | capsule | Marketed | Teva Pharms |
| Prozac | United States | 10MG BASE, 20MG BASE, 40MG BASE … | capsule | Not marketed | Eli Lilly and Co |
| Sarafem | United States | 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | capsule | Not marketed | Eli Lilly and Co |
| Prozac | United States | 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | tablet | Not marketed | Lilly |
| Prozac | United States | 20MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | solution | Not marketed | Lilly |
| Prozac Weekly | United States | 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | capsule, delayed rel pellets | Not marketed | Lilly |
| Sarafem | United States | 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | tablet | Not marketed | Apil |
| Selfemra | United States | 10MG BASE, 15MG BASE, 20MG BASE | tablet | Not marketed | Teva Pharms USA |
| SymbyaxCombination | United States | 25MG BASE; 12MG BASE, 25MG BASE; 3MG BASE, 25MG BASE; 6MG BASE … | capsule | Not marketed | Lilly |
The same brand on several registers.
The companies holding its medicines, the most first.
Substances it shares a medicine with.
How the registers write it, in their own languages.
Compiled by Prognia from the public medicine registers of AEMPS, AIFA, ALIMS, Anvisa, CBG-MEB, EMA, FDA, HALMED, Health Canada, HSA, MS, PHARMAC and SFDA. 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.
