NDC11 00135019602
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 |
|---|---|
| 00135-0196-02 | 00135-0196 |
| 00135-0196-2 | 00135-0196 |
| 00135-196-02 | 00135-196 |
| 0135-0196-02 | 0135-0196 |
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 |
|---|---|---|---|---|---|---|
| NICODERM CQ | NICOTINE | Haleon US Holdings LLC | 93b2d1b9-83c1-40b5-b6af-90c38c8d6cef | 2025-07-14 | Warnings | 0135-0196-02 0135-0196 00135019602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.