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Fluoxetine
FLUOXETINE HYDROCHLORIDE
Active ingredient 14 prescription 32 with labelling
Overview
Source: NDC DirectoryIngredient name
FLUOXETINE HYDROCHLORIDE
Base moiety
FLUOXETINE
RxNorm CUI
UNII
I9W7N6B1KJ
Medication products
19
Brand names
7
Dosage forms
9
FAERS reports
126,825 · not a risk measure
- Fluoxetine Powder
- Fluoxetine HCl Powder
- Fluoxetine hydrochloride Capsule
- Fluoxetine Hydrochloride Powder
- Fluoxetine Hydrochloride Solution
- Fluoxetine Hydrochloride Capsule, Delayed Release Pellets
- Fluoxetine hydrochloride For Solution
- Fluoxetine Hydrochloride Process II Powder
- Fluoxetine Tablet, Film Coated
- Fluoxetine Fluoxetine Hydrochloride · Capsule
- Fluoxetine Fluoxetine Hydrochloride · Solution
- fluoxetine Tablet
- Fluoxetine Liquid
- Fluoxetine HCL Capsule
- fluoxetine hydrochloride Tablet, Coated
- Fluoxetine Hydrochloride Tablet, Film Coated
- Fluoxetine Hydrochloride Tablet
- Olanzapine and Fluoxetine Capsule
- Prozac Fluoxetine hydrochloride · Capsule
Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.
By dosage form
| Dosage form | Products | Examples |
|---|---|---|
| Capsule | 5 | Fluoxetine hydrochloride, Fluoxetine, Fluoxetine HCL, Olanzapine and Fluoxetine … |
| Powder | 4 | Fluoxetine, Fluoxetine HCl, Fluoxetine Hydrochloride, Fluoxetine Hydrochloride Process II |
| Solution | 2 | Fluoxetine Hydrochloride, Fluoxetine |
| TABLET, Film Coated | 2 | Fluoxetine, Fluoxetine Hydrochloride |
| Tablet | 2 | fluoxetine, Fluoxetine Hydrochloride |
| CAPSULE, Delayed Release Pellets | 1 | Fluoxetine Hydrochloride |
| For Solution | 1 | Fluoxetine hydrochloride |
| Liquid | 1 | Fluoxetine |
| TABLET, Coated | 1 | fluoxetine hydrochloride |
Sources for this page
| Dataset | Agency | Used for |
|---|---|---|
| NDC Directory | FDA | Ingredient name, strengths, products, labelers, packages |
| DailyMed RxNorm mappings | NLM | RxNorm concept identifier (RxCUI) |
| FAERS | FDA | Adverse event report totals |