NDC11 49483072001
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 |
|---|---|
| 49483-0720-01 | 49483-0720 |
| 49483-0720-1 | 49483-0720 |
| 49483-720-01 | 49483-720 |
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 |
|---|---|---|---|---|---|---|
| Maximum Strength Acid Reducer | FAMOTIDINE | TIME CAP LABORATORIES,INC | fe25e1e2-7158-6fe0-e053-6394a90a3bb1 | 2024-03-06 | Warnings | 49483-720-01 49483-720 49483072001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.