Sumatriptan Succinate
- Product NDC
- 70518-2859
- 11-digit product format
- 705182859
- Labeler code
- 70518
- Product ID
- 70518-2859_d7724276-e524-5af3-e053-2a95a90ae5a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076847
- Marketing category
- ANDA
- Marketing start
- 2020-08-26
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 50 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2859-0 | 70518285900 | 9 BLISTER PACK in 1 CARTON (70518-2859-0) > 1 TABLET in 1 BLISTER PACK | 9 blister pack | 2020-08-26 | 0000-00-00 | No | No | Current |