NDC11 53489014405
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 53489-0144-05 | 53489-0144 |
| 53489-0144-5 | 53489-0144 |
| 53489-144-05 | 53489-144 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Spironolactone and Hydrochlorothiazide | SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE | Sun Pharmaceutical Industries, Inc. | d7fa3c79-9f26-415b-8039-eb2acabcf66b | 2025-12-09 | Warnings, Adverse reactions | 53489-144-05 53489-144 53489014405 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.