Sumatriptan Succinate
- Product NDC
- 76420-093
- 11-digit product format
- 764200093
- Labeler code
- 76420
- Product ID
- 76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA076847
- Marketing category
- ANDA
- Marketing start
- 2009-11-17
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 50 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-093-09 | 76420009309 | 9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 TABLET in 1 BLISTER PACK | 9 blister pack | 2020-10-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sumatriptan Succinate | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2020-10-24 | HUMAN PRESCRIPTION DRUG LABEL | 1 |