NDC11 29300013501
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 |
|---|---|
| 29300-0135-01 | 29300-0135 |
| 29300-0135-1 | 29300-0135 |
| 29300-135-01 | 29300-135 |
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 | 29300-135 | 29300-135-01 | D | Discontinued by firm | 2026-08-07 |
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 |
|---|---|---|---|---|---|---|
| clonidine hydrochloride | CLONIDINE HYDROCHLORIDE | Unichem Pharmaceuticals (USA), Inc. | 21bfa28f-20df-43fd-bb80-b720d3b40696 | 2026-03-30 | Warnings, Adverse reactions | 29300-135-01 29300-135 29300013501 |