Sumatriptan Succinate
- Product NDC
- 72189-596
- 11-digit product format
- 721890596
- Labeler code
- 72189
- Product ID
- 72189-596_284ee7ac-759f-b592-e063-6394a90a78ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078284
- Marketing category
- ANDA
- Marketing start
- 2024-12-02
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 25 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| J8BDZ68989 | SUMATRIPTAN SUCCINATE | 103628-48-4 | SUMATRIPTAN SUCCINATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-596-09 | 72189059609 | 9 TABLET, FILM COATED in 1 CARTON (72189-596-09) | 2024-12-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sumatriptan Succinate | Direct_Rx | 2024-12-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |