NDC11 53489032906
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 |
|---|---|
| 53489-0329-06 | 53489-0329 |
| 53489-0329-6 | 53489-0329 |
| 53489-329-06 | 53489-329 |
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 53489-329 | 53489-329-06 | D | Discontinued by firm | 2026-08-11 |
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 | SPIRONOLACTONE | Sun Pharmaceutical Industries, Inc. | c23b6b9b-aec3-48a8-a518-76e4097f6479 | 2026-07-31 | Warnings, Adverse reactions | 53489-329-06 53489-329 53489032906 |