NDC 59115-092-55 - Risperidone
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 59115-092
- Requested NDC
- 59115-092-55
- Package NDCs from labels
- 59115-092-55, 59115-092-60
- Manufacturer
- Hikma Pharmaceutical | Al Hikma Pharmaceuticals LLC
- Effective date
- 2011-08-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Risperidone - Hikma Pharmaceutical | Al Hikma Pharmaceuticals LLC | Hikma Pharmaceutical | Al Hikma Pharmaceuticals LLC | 2011-08-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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| risperidone | RISPERIDONE | Cardinal Health 107, LLC | 3ce21196-4aa0-469b-8f04-6650b2c48cb5 | 2026-04-07 | Boxed warning, Warnings, Adverse reactions | L6UH7ZF8HC |
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| Clinical Skin Filter Tinted Sunscreen | CLINICAL SKIN FILTER TINTED SUNSCREEN | BY KIN AESTHETICS LLC | 4e69a8a3-8dbb-577a-e063-6294a90a6a23 | 2026-04-01 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.