Sumatriptan
- Product NDC
- 76420-499
- 11-digit product format
- 764200499
- Labeler code
- 76420
- Product ID
- 76420-499_eacf382a-98ac-e3ad-e053-2995a90a44e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA078327
- Marketing category
- ANDA
- Marketing start
- 2009-08-17
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sumatriptan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUMATRIPTAN SUCCINATE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J8BDZ68989 |
| Rxcui | 313160, 313161, 315223 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-499-09 | Sumatriptan | 9 in 1 BLISTER PACK | TABLET | 9 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-499 | SUMATRIPTAN (SUMATRIPTAN SUCCINATE) TABLET [ASCLEMED USA, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20221013_77f9f135-e840-48f0-81e8-73e08433e768.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-499-09 | 76420049909 | 9 TABLET in 1 BLISTER PACK (76420-499-09) | 9 tablet | 2022-10-12 | 0000-00-00 | No | No | Current |