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Rizatriptan Benzoate - 47335-231-18 - (Rizatriptan Benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 47335-231
Proprietary Name: Rizatriptan Benzoate
Non Proprietary Name: Rizatriptan Benzoate
Active Ingredient(s): 5    mg/1 & nbsp;   Rizatriptan Benzoate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Rizatriptan Benzoate

Product NDC: 47335-231
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202047
Marketing Category: ANDA
Start Marketing Date: 20130112

Package Information of Rizatriptan Benzoate

Package NDC: 47335-231-18
Package Description: 1000 TABLET in 1 BOTTLE (47335-231-18)

NDC Information of Rizatriptan Benzoate

NDC Code 47335-231-18
Proprietary Name Rizatriptan Benzoate
Package Description 1000 TABLET in 1 BOTTLE (47335-231-18)
Product NDC 47335-231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan Benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130112
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name RIZATRIPTAN BENZOATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of Rizatriptan Benzoate


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