NDC11 00135009070
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 |
|---|---|
| 00135-0090-70 | 00135-0090 |
| 00135-090-70 | 00135-090 |
| 0135-0090-70 | 0135-0090 |
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 |
|---|---|---|---|---|---|---|
| CITRUCEL | METHYLCELLULOSE | Haleon US Holdings LLC | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 2026-03-18 | Warnings | 0135-0090-70 0135-0090 00135009070 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.