Sumatriptan
- Product NDC
- 55700-759
- 11-digit product format
- 557000759
- Labeler code
- 55700
- Product ID
- 55700-759_c7356307-4040-4541-aeb4-b8ebc9515c2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078327
- Marketing category
- ANDA
- Marketing start
- 2019-05-24
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 25 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-759-09 | 55700075909 | 1 BLISTER PACK in 1 CARTON (55700-759-09) > 9 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-05-24 | 0000-00-00 | No | No | Current |