NDC11 42571013360
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 |
|---|---|
| 42571-0133-60 | 42571-0133 |
| 42571-133-60 | 42571-133 |
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 |
|---|---|---|---|---|---|---|
| Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL | DICLOFENAC SODIUM/MISOPROSTOL | Micro Labs Limited | c61df58d-d6bb-4d3e-9ef8-60caa7d4e762 | 2025-07-28 | Boxed warning, Warnings, Adverse reactions | 42571-133-60 42571-133 42571013360 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.