Zolmitriptan
- Product NDC
- 55801-322
- 11-digit product format
- 558010322
- Labeler code
- 55801
- Product ID
- 55801-322_e53c9020-5583-47f8-9039-752abd023cea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolmitriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- APPCO PHARMA LLC
- Application
- ANDA206973
- Marketing category
- ANDA
- Marketing start
- 2017-09-15
- Marketing end
- 0000-00-00
- Substance
- ZOLMITRIPTAN
- Active strength
- 3 mg/1
- Pharmacologic classes
- Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record