NDC11 50804012922
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 |
|---|---|
| 50804-0129-22 | 50804-0129 |
| 50804-129-22 | 50804-129 |
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 |
|---|---|---|---|---|---|---|
| GoodSense Extra Strength Antacid | CALCIUM CARBONATE | GoodSense | 2fcdeb06-17de-49d8-97bb-8d31e1c0c61f | 2025-01-20 | Warnings | 50804-129-22 50804-129 50804012922 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.