Rizatriptan Benzoate

Product NDC
71335-1172
11-digit product format
713351172
Labeler code
71335
Product ID
71335-1172_dcf0ec97-3206-4fb8-8ede-14664e69d5a5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rizatriptan Benzoate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207836
Marketing category
ANDA
Marketing start
2017-03-07
Marketing end
0000-00-00
Substance
RIZATRIPTAN BENZOATE
Active strength
10 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
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1172-17133511720110 TABLET in 1 BOTTLE (71335-1172-1) 10 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-2713351172026 TABLET in 1 BOTTLE (71335-1172-2) 6 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-37133511720390 TABLET in 1 BOTTLE (71335-1172-3) 90 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-4713351172049 TABLET in 1 BOTTLE (71335-1172-4) 9 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-57133511720530 TABLET in 1 BOTTLE (71335-1172-5) 30 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-67133511720618 TABLET in 1 BOTTLE (71335-1172-6) 18 tablet2019-04-030000-00-00NoNoCurrent
71335-1172-77133511720712 TABLET in 1 BOTTLE (71335-1172-7) 12 tablet2019-04-030000-00-00NoNoCurrent