sumatriptan
- Product NDC
- 83270-151
- 11-digit product format
- 832700151
- Labeler code
- 83270
- Product ID
- 83270-151_4b3f1ed8-151c-79f2-e063-6394a90ada00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Application
- ANDA090314
- Marketing category
- ANDA
- Marketing start
- 2026-02-02
- 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 | 727339, 1657151 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83270-151-07 | sumatriptan | 0.5 mL in 1 SYRINGE | INJECTION, SOLUTION | 0.5 | | 2 |
| 83270-151-07 | sumatriptan | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83270-151-07 | 83270015107 | 2 SYRINGE in 1 CARTON (83270-151-07) / .5 mL in 1 SYRINGE | 2 syringe | 2026-02-02 | No | No | Current |