NDC11 48951909201
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 |
|---|---|
| 48951-9092-01 | 48951-9092 |
| 48951-9092-1 | 48951-9092 |
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 | 48951-9092 | 48951-9092-1 | I | Inactivated by FDA | 2026-08-17 |
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 |
|---|---|---|---|---|---|---|
| Viscum Mali e pl. tota 4 | VISCUM MALI E PL. TOTA 4 | Uriel Pharmacy Inc. | aea0e043-f04a-4f42-975e-47a80963c933 | 2026-08-21 | Warnings | 48951-9092-1 48951-9092 48951909201 |