NDC11 51662134102
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 |
|---|---|
| 51662-1341-02 | 51662-1341 |
| 51662-1341-2 | 51662-1341 |
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 |
|---|---|---|---|---|---|---|
| AMINOPHYLLINE | AMINOPHYLLINE | HF Acquisition Co LLC, DBA HealthFirst | 819207a2-0c37-b275-e053-2a91aa0afb36 | 2026-06-19 | Warnings, Adverse reactions | 51662-1341-2 51662-1341 51662134102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.