NDC11 63548019702
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 |
|---|---|
| 63548-0197-02 | 63548-0197 |
| 63548-0197-2 | 63548-0197 |
| 63548-197-02 | 63548-197 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen 200 mg and Diphenhydramine Citrate 38 mg | IBUPROFEN, DIPHENHYDRAMINE CITRATE | PLD Acquisitions LLC DBA Avma Pharma Solutions | a7d729bf-6d7a-415a-a414-cae0ba6d0063 | 2024-04-24 | Warnings | 63548-0197-2 63548-0197 63548019702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.