Relpax
- Product NDC
- 58151-367
- 11-digit product format
- 581510367
- Labeler code
- 58151
- Product ID
- 58151-367_ca50a848-b287-47b6-980b-5729d4582893
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eletriptan hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Viatris Specialty LLC
- Application
- NDA021016
- Marketing category
- NDA
- Marketing start
- 2025-05-08
- Substance
- ELETRIPTAN HYDROBROMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Relpax
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ELETRIPTAN HYDROBROMIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | M41W832TA3 |
| Rxcui | 359493, 359494, 404443, 404444 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58151-367-56 | Relpax | 6 in 1 CARTON | TABLET | 6 | | 4 |
| 58151-367-56 | Relpax | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58151-367 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET [VIATRIS SPECIALTY LLC] | 4 | Current NDC, 2 package rows | 20250510_2a501dbd-3ea8-47e4-9fcb-07035b8c8c9e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58151-367-56 | 58151036756 | 6 BLISTER PACK in 1 CARTON (58151-367-56) / 1 TABLET in 1 BLISTER PACK | 6 blister pack | 2025-05-08 | No | No | Current |