Sumatriptan
- Product NDC
- 55700-918
- 11-digit product format
- 557000918
- Labeler code
- 55700
- Product ID
- 55700-918_8689443c-5dc1-4338-bb5d-7406930518ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078284
- Marketing category
- ANDA
- Marketing start
- 2021-07-22
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-918-09 | 55700091809 | 9 TABLET, FILM COATED in 1 BLISTER PACK (55700-918-09) | 2021-07-22 | 0000-00-00 | No | No | Current |