NDC11 83324021901
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 |
|---|---|
| 83324-0219-01 | 83324-0219 |
| 83324-0219-1 | 83324-0219 |
| 83324-219-01 | 83324-219 |
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 |
|---|---|---|---|---|---|---|
| QUALITY CHOICE Original Flavor | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | CHAIN DRUG MARKETING ASSOCIATION INC. | a699b830-6400-4af9-9810-5eda79157333 | 2025-12-04 | Warnings | 83324-219-01 83324-219 83324021901 |