Rizatriptan Benzoate

Product NDC
71335-2536
11-digit product format
713352536
Labeler code
71335
Product ID
71335-2536_9fd5b7a4-8fbb-417f-9deb-b692d7db3cb9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rizatriptan Benzoate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202490
Marketing category
ANDA
Marketing start
2012-12-31
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WR978S7QHHRIZATRIPTAN BENZOATE145202-66-0RIZATRIPTAN BENZOATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2536-17133525360130 TABLET in 1 BLISTER PACK (71335-2536-1) 30 tablet2024-12-10NoNoHistorical
71335-2536-27133525360218 TABLET in 1 BLISTER PACK (71335-2536-2) 18 tablet2024-12-10NoNoHistorical
71335-2536-37133525360312 TABLET in 1 BLISTER PACK (71335-2536-3) 12 tablet2024-12-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rizatriptan BenzoateBryant Ranch Prepack2024-12-10HUMAN PRESCRIPTION DRUG LABEL1