sumatriptan succinate
- Product NDC
- 71205-725
- 11-digit product format
- 712050725
- Labeler code
- 71205
- Product ID
- 71205-725_f23ac454-8f7d-4c1b-be58-a394c8b0a966
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078295
- Marketing category
- ANDA
- Marketing start
- 2009-08-10
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-725 | SUMATRIPTAN SUCCINATE TABLET, FILM COATED [PROFICIENT RX LP] | 1 | Legacy NDC | 20221202_f23ac454-8f7d-4c1b-be58-a394c8b0a966.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-725-09 | 71205072509 | 9 BLISTER PACK in 1 CARTON (71205-725-09) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 9 blister pack | 2022-11-30 | 0000-00-00 | No | No | Current |
| 71205-725-30 | 71205072530 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-725-30) | | 2022-11-30 | 0000-00-00 | No | No | Current |
| 71205-725-60 | 71205072560 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-725-60) | | 2022-11-30 | 0000-00-00 | No | No | Current |
| 71205-725-90 | 71205072590 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-725-90) | | 2022-11-30 | 0000-00-00 | No | No | Current |