Sumatriptan
- Product NDC
- 50090-7957
- 11-digit product format
- 500907957
- Labeler code
- 50090
- Product ID
- 50090-7957_e2480832-60c7-4cb7-93b0-90267baa8c70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA213998
- Marketing category
- ANDA
- Marketing start
- 2024-09-28
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 6 mg/.5mL
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sumatriptan
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUMATRIPTAN SUCCINATE | 6 mg/.5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J8BDZ68989 |
| Rxcui | 313165 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7957-0 | Sumatriptan | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | | 1 |
| 50090-7957-0 | Sumatriptan | .5 mL in 1 VIAL | INJECTION, SOLUTION | .5 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7957-0 | 50090795700 | 5 VIAL in 1 CARTON (50090-7957-0) / .5 mL in 1 VIAL | 5 vial | 2026-05-04 | No | No | Historical |