NDC 52389-656-01 - Diurex Ultimate
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
- 52389-656
- Requested NDC
- 52389-656-01
- Package NDCs from labels
- 52389-656-01, 52389-656-60
- Manufacturer
- Kobayashi Healthcare International, Inc. | Kobayashi America Manufacturing, LLC
- Effective date
- 2026-06-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diurex Ultimate | Kobayashi Healthcare International, Inc. | Kobayashi America Manufacturing, LLC | 2026-06-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52389-656-01 | DiurexUltimate | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 12 | |
| 52389-656-60 | DiurexUltimate | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 12 |
DailyMed Dashboard NDC Coverage#
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.