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Rizatriptan Benzoate - 0093-7471-43 - (Rizatriptan Benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 0093-7471
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: 0093-7471
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077263
Marketing Category: ANDA
Start Marketing Date: 20130212

Package Information of Rizatriptan Benzoate

Package NDC: 0093-7471-43
Package Description: 18 BLISTER PACK in 1 BOX (0093-7471-43) > 1 TABLET in 1 BLISTER PACK (0093-7471-19)

NDC Information of Rizatriptan Benzoate

NDC Code 0093-7471-43
Proprietary Name Rizatriptan Benzoate
Package Description 18 BLISTER PACK in 1 BOX (0093-7471-43) > 1 TABLET in 1 BLISTER PACK (0093-7471-19)
Product NDC 0093-7471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan Benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130212
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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