NDC 71335-1352

Rizatriptan

Rizatriptan

Rizatriptan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Rizatriptan Benzoate.

Product ID71335-1352_003d054f-41a7-4256-a173-275ef9fb3578
NDC71335-1352
Product TypeHuman Prescription Drug
Proprietary NameRizatriptan
Generic NameRizatriptan
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2014-03-11
Marketing CategoryANDA / ANDA
Application NumberANDA203147
Labeler NameBryant Ranch Prepack
Substance NameRIZATRIPTAN BENZOATE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-1352-1

10 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-1)
Marketing Start Date2022-09-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1352-4 [71335135204]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-03-11

NDC 71335-1352-1 [71335135201]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11

NDC 71335-1352-5 [71335135205]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11

NDC 71335-1352-2 [71335135202]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11

NDC 71335-1352-6 [71335135206]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11

NDC 71335-1352-3 [71335135203]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11

NDC 71335-1352-7 [71335135207]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-10-02

Drug Details

Active Ingredients

IngredientStrength
RIZATRIPTAN BENZOATE10 mg/1

Pharmacological Class

  • Serotonin 1b Receptor Agonists [MoA]
  • Serotonin 1d Receptor Agonists [MoA]
  • Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

NDC Crossover Matching brand name "Rizatriptan" or generic name "Rizatriptan"

NDCBrand NameGeneric Name
33342-087RizatriptanRizatriptan
33342-088RizatriptanRizatriptan
71335-1352RizatriptanRizatriptan
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