NDC 33342-088

Rizatriptan

Rizatriptan

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

Product ID33342-088_56501917-d17b-4912-8a4b-6a4690115eae
NDC33342-088
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 NameMacleods Pharmaceuticals Limited
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 Through2021-12-31

Packaging

NDC 33342-088-07

30 TABLET, FILM COATED in 1 CONTAINER (33342-088-07)
Marketing Start Date2014-03-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 33342-088-41 [33342008841]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-09-03

NDC 33342-088-72 [33342008872]

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

NDC 33342-088-02 [33342008802]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-09-03

NDC 33342-088-12 [33342008812]

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

NDC 33342-088-52 [33342008852]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-07

NDC 33342-088-07 [33342008807]

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

NDC 33342-088-46 [33342008846]

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

NDC 33342-088-45 [33342008845]

Rizatriptan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203147
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-09-03

NDC 33342-088-50 [33342008850]

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

Drug Details

Active Ingredients

IngredientStrength
RIZATRIPTAN BENZOATE10 mg/1

OpenFDA Data

SPL SET ID:27bc2cfc-fefb-4b50-a0dc-6268c69b4902
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314209
  • 312840
    • UPC Code
  • 0777742028462

    • Pharmacological Class

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

    Medicade Reported Pricing

    33342008872 RIZATRIPTAN 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    33342008850 RIZATRIPTAN 10 MG TABLET

    Pricing Unit: EA | Drug Type:

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

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