NDC11 48951139603
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 |
|---|---|
| 48951-1396-03 | 48951-1396 |
| 48951-1396-3 | 48951-1396 |
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 |
|---|---|---|---|---|---|---|
| Amnion Oxalis comp. | AMNION OXALIS COMP. | Uriel Pharmacy, Inc | 2d7f3585-002b-854b-e063-6294a90ab9fa | 2025-02-06 | Warnings | 48951-1396-3 48951-1396 48951139603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.