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Prednisone
Active ingredient 8 prescription 14 with labelling
Overview
Source: NDC DirectoryIngredient name
PREDNISONE
Base moiety
PREDNISONE
RxNorm CUI
UNII
VB0R961HZT
Medication products
11
Brand names
8
Dosage forms
5
FAERS reports
499,957 · not a risk measure
- Prednisone Powder
- Prednisone Anhydrous Powder
- PredniSONE Intensol Solution, Concentrate
- PREDNISONE MICRONIZED ANHYDROUS Prednisone Micronized Anhydrous · Powder
- Prednisone Tablet
- PredniSONE Solution
- Prednisone D/P Tablet
- Prednisone delayed release Prednisone · Tablet, Delayed Release
- PredniSONE Tablets, USP, 10 mg PredniSONE · Tablet
- PredniSONE Tablets, USP, 20 mg PredniSONE · Tablet
- PredniSONE Tablets, USP, 5 mg PredniSONE · Tablet
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 |
|---|---|---|
| Tablet | 5 | Prednisone, Prednisone D/P, PredniSONE Tablets, USP, 10 mg, PredniSONE Tablets, USP, 20 mg … |
| Powder | 3 | Prednisone, Prednisone Anhydrous, PREDNISONE MICRONIZED ANHYDROUS |
| SOLUTION, Concentrate | 1 | PredniSONE Intensol |
| Solution | 1 | PredniSONE |
| TABLET, Delayed Release | 1 | Prednisone delayed release |
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 |