sumatriptan succinate
- Product NDC
- 55700-092
- 11-digit product format
- 557000092
- Labeler code
- 55700
- Product ID
- 55700-092_7bd2e76b-500f-4493-8480-2561c42a7b10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078295
- Marketing category
- ANDA
- Marketing start
- 2009-08-10
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record