Sumatriptan
- Product NDC
- 42043-221
- 11-digit product format
- 420430221
- Labeler code
- 42043
- Product ID
- 42043-221_bcca2aac-a52e-4a0c-b5be-2cf62be34a12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- OrchidPharma Inc
- Application
- ANDA078284
- Marketing category
- ANDA
- Marketing start
- 2020-03-04
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 50 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
- 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 |
|---|
| 42043-221-09 | 42043022109 | 1 BLISTER PACK in 1 CARTON (42043-221-09) > 9 TABLET, FILM COATED in 1 BLISTER PACK (42043-221-00) | 1 blister pack | 2020-03-04 | 0000-00-00 | No | No | Current |