NDC11 61727033421
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 |
|---|---|
| 61727-0334-21 | 61727-0334 |
| 61727-334-21 | 61727-334 |
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 |
|---|---|---|---|---|---|---|
| Leg Cramps Relief | CUPRIC ARSENITE, COPPER, POTASSIUM PHOSPHATE, DIBASIC, LACTIC ACID, L-,MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE | Homeocare Laboratories | e34601fb-2bd8-498a-9910-d82410e93036 | 2018-12-31 | Warnings | 61727-334-21 61727-334 61727033421 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.