Sumatriptan
- Product NDC
- 68071-4061
- 11-digit product format
- 680714061
- Labeler code
- 68071
- Product ID
- 68071-4061_bb2bf1f1-be83-f4cf-e053-2995a90afd0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate U-D
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078327
- Marketing category
- ANDA
- Marketing start
- 2009-08-17
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-4061-9 | 68071406109 | 9 TABLET in 1 BOX (68071-4061-9) | 9 tablet | 2017-08-21 | 0000-00-00 | No | No | Current |