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Rizatriptan Benzoate - 65862-599-12 - (Rizatriptan Benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 65862-599
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: 65862-599
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202490
Marketing Category: ANDA
Start Marketing Date: 20121231

Package Information of Rizatriptan Benzoate

Package NDC: 65862-599-12
Package Description: 4 BLISTER PACK in 1 CARTON (65862-599-12) > 3 TABLET in 1 BLISTER PACK (65862-599-03)

NDC Information of Rizatriptan Benzoate

NDC Code 65862-599-12
Proprietary Name Rizatriptan Benzoate
Package Description 4 BLISTER PACK in 1 CARTON (65862-599-12) > 3 TABLET in 1 BLISTER PACK (65862-599-03)
Product NDC 65862-599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan Benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121231
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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