NDC11 43598000801
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 |
|---|---|
| 43598-0008-01 | 43598-0008 |
| 43598-0008-1 | 43598-0008 |
| 43598-008-01 | 43598-008 |
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 |
|---|---|---|---|---|---|---|
| Guaifenesin 600 mg | GUAIFENESIN | Dr. Reddy's Laboratories Inc. | 99307c61-5df3-0a83-1e21-ddb03bc905b4 | 2024-07-26 | Warnings | 43598-008-01 43598-008 43598000801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.