sumatriptan succinate
- Product NDC
- 42023-121
- 11-digit product format
- 420230121
- Labeler code
- 42023
- Product ID
- 42023-121_602f8636-913b-4686-9f3f-b625b44b7a89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- JHP Pharmaceuticals LLC
- Application
- ANDA077871
- Marketing category
- ANDA
- Marketing start
- 2009-08-06
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 6 mg/.5mL
- Pharmacologic classes
- Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#