NDC11 83324012112
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 |
|---|---|
| 83324-0121-12 | 83324-0121 |
| 83324-121-12 | 83324-121 |
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 |
|---|---|---|---|---|---|---|
| QCH Regular Strength Antacid 509 | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | Chain Drug Marketing Association Inc. | 17947ccd-6f11-d4cd-e063-6294a90a108a | 2024-08-27 | Warnings | 83324-121-12 83324-121 83324012112 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.