NDC11 52536005903
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 |
|---|---|
| 52536-0059-03 | 52536-0059 |
| 52536-0059-3 | 52536-0059 |
| 52536-059-03 | 52536-059 |
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 |
|---|---|---|---|---|---|---|
| Amphetamine Sulfate | AMPHETAMINE SULFATE | Wilshire Pharmaceuticals, Inc. | 91add2e3-8359-47dc-b79f-197d36b02819 | 2025-10-24 | Boxed warning, Warnings, Adverse reactions | 52536-059-03 52536-059 52536005903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.