Rizatriptan Benzoate
- Product NDC
- 0781-5425
- 11-digit product format
- 007815425
- Labeler code
- 0781
- Product ID
- 0781-5425_20d6135d-6da3-4e3b-8337-6e9635c8aadb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rizatriptan benzoate
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA078739
- Marketing category
- ANDA
- Marketing start
- 2013-07-02
- Marketing end
- 0000-00-00
- Substance
- RIZATRIPTAN BENZOATE
- Active strength
- 5 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record