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rizatriptan benzoate - 68462-467-06 - (rizatriptan benzoate)

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Drug Information of rizatriptan benzoate

Product NDC: 68462-467
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, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of rizatriptan benzoate

Product NDC: 68462-467
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201914
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of rizatriptan benzoate

Package NDC: 68462-467-06
Package Description: 6 BOX in 1 CARTON (68462-467-06) > 3 POUCH in 1 BOX > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of rizatriptan benzoate

NDC Code 68462-467-06
Proprietary Name rizatriptan benzoate
Package Description 6 BOX in 1 CARTON (68462-467-06) > 3 POUCH in 1 BOX > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 68462-467
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rizatriptan benzoate
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
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]

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