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Esomeprazole
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
Active ingredient 3 prescription 5 over-the-counter 13 with labelling
Overview
Source: NDC DirectoryIngredient name
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
Base moiety
ESOMEPRAZOLE
RxNorm CUI
UNII
36H71644EQ
Medication products
14
Brand names
6
Dosage forms
5
FAERS reports
235,236 · not a risk measure
- Esomeprazole Magnesium Powder
- Esomeprazole Magnesium Dihydrate Powder
- Esomeprazole Magnesium Dihydrate Process II Powder
- ESOMEPRAZOLE MAGNESIUM MINIS esomeprazole magnesium dihydrate · Capsule, Delayed Release
- Esomeprazole Magnesium Trihydrate Powder
- Esomeprazole Mg Dihydrate Powder
- Esomeprazole mgdi micro Powder
- topcare esomeprazole magnesium esomeprazole magnesium · Capsule, Delayed Release
- equate esomeprazole magnesium esomeprazole magnesium dihydrate · Capsule, Delayed Release
- Esomeprazole Magnesium Capsule, Delayed Release
- Esomeprazole Magnesium Granule, Delayed Release
- Esomeprazole Magnesium Tablet, Delayed Release
- Esomeprazole magnesium For Suspension
- Up and Up Esomeprazole Magnesium esomeprazole magnesium · Capsule, Delayed Release
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 |
|---|---|---|
| Powder | 6 | Esomeprazole Magnesium, Esomeprazole Magnesium Dihydrate, Esomeprazole Magnesium Dihydrate Process II, Esomeprazole Magnesium Trihydrate … |
| CAPSULE, Delayed Release | 5 | ESOMEPRAZOLE MAGNESIUM MINIS, topcare esomeprazole magnesium, equate esomeprazole magnesium, Esomeprazole Magnesium … |
| GRANULE, Delayed Release | 1 | Esomeprazole Magnesium |
| TABLET, Delayed Release | 1 | Esomeprazole Magnesium |
| For Suspension | 1 | Esomeprazole magnesium |
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 |