Sumatriptan
- Product NDC
- 68071-2825
- 11-digit product format
- 680712825
- Labeler code
- 68071
- Product ID
- 68071-2825_e7b5cc69-25a4-3d5e-e053-2995a90a0b78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078284
- Marketing category
- ANDA
- Marketing start
- 2022-02-18
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 100 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2825-9 | Sumatriptan | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 1 |
| 68071-2825-9 | Sumatriptan | 9 in 1 BLISTER PACK | TABLET, FILM COATED | 9 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2825 | SUMATRIPTAN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 2 package rows | 20220904_e7b5cc62-0531-751e-e053-2a95a90aa26f.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 |
|---|
| 68071-2825-9 | 68071282509 | 1 BLISTER PACK in 1 CARTON (68071-2825-9) > 9 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2022-09-02 | 0000-00-00 | No | No | Current |