NDC 59651-105-06 - Eletriptan HBR
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 59651-105
- Requested NDC
- 59651-105-06
- Package NDCs from labels
- 59651-105-06, 59651-105-69, 59651-105-93
- Manufacturer
- Direct_Rx
- Effective date
- 2025-01-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Eletriptan HBR - Direct_Rx | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Eletriptan Hydrobromide - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-09-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Eletriptan Hydrobromide - Advanced Rx of Tennessee, LLC | Advanced Rx of Tennessee, LLC | 2024-06-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Eletriptan Hydrobromide - Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | 2024-06-03 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59651-105-06 | Eletriptan Hydrobromide | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | 5 | |
| 59651-105-69 | Eletriptan Hydrobromide | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 5 | |
| 59651-105-93 | Eletriptan Hydrobromide | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 5 | |
| 59651-105-93 | Eletriptan Hydrobromide | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 59651-105-06 | EA - Each | 59651-105 | a5de6b8e-5077-4ec6-8e0c-4ba9fdc85a6f | 1 | 2019-04-11 |
| 59651-105-69 | EA - Each | 59651-105 | 783cc77f-2b7a-4d78-a85f-6f9f7c2cb004 | 1 | 2019-04-11 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.