Rizatriptan Benzoate

Product NDC
51991-354
11-digit product format
519910354
Labeler code
51991
Product ID
51991-354_d48d54bc-d3a2-47bb-8959-65f6837d1c33
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rizatriptan Benzoate
Dosage form
TABLET
Route
ORAL
Labeler
Breckenridge Pharmaceutical, Inc.
Application
ANDA200482
Marketing category
ANDA
Marketing start
2012-12-31
Marketing end
2024-07-31
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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51991-354-78EA - Each51991-3544d9a1c08-7f33-43b3-ae0b-9669999b060a12013-02-13
51991-354-99EA - Each51991-354d029563a-1b2e-444f-8daf-eb4c7711a96f12013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51991-354-785199103547818 BLISTER PACK in 1 CARTON (51991-354-78) > 6 TABLET in 1 BLISTER PACK (51991-354-99) 18 blister pack2012-12-310000-00-00NoNoCurrent