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Rizatriptan Benzoate - 54868-6397-1 - (rizatriptan benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 54868-6397
Proprietary Name: Rizatriptan Benzoate
Non Proprietary Name: rizatriptan benzoate
Active Ingredient(s): 10    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: 54868-6397
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078173
Marketing Category: ANDA
Start Marketing Date: 20130129

Package Information of Rizatriptan Benzoate

Package NDC: 54868-6397-1
Package Description: 9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (54868-6397-1)

NDC Information of Rizatriptan Benzoate

NDC Code 54868-6397-1
Proprietary Name Rizatriptan Benzoate
Package Description 9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (54868-6397-1)
Product NDC 54868-6397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rizatriptan benzoate
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130129
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name RIZATRIPTAN BENZOATE
Strength Number 10
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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