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Rizatriptan benzoate - 0781-5485-64 - (Rizatriptan benzoate)

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Drug Information of Rizatriptan benzoate

Product NDC: 0781-5485
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: 0781-5485
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079230
Marketing Category: ANDA
Start Marketing Date: 20130211

Package Information of Rizatriptan benzoate

Package NDC: 0781-5485-64
Package Description: 3 BLISTER PACK in 1 CARTON (0781-5485-64) > 10 TABLET in 1 BLISTER PACK

NDC Information of Rizatriptan benzoate

NDC Code 0781-5485-64
Proprietary Name Rizatriptan benzoate
Package Description 3 BLISTER PACK in 1 CARTON (0781-5485-64) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-5485
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130211
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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