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Rizatriptan Benzoate - 0378-1404-05 - (rizatriptan benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 0378-1404
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
Coding System: National Drug Codes(NDC)

Labeler Information of Rizatriptan Benzoate

Product NDC: 0378-1404
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201993
Marketing Category: ANDA
Start Marketing Date: 20121231

Package Information of Rizatriptan Benzoate

Package NDC: 0378-1404-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0378-1404-05)

NDC Information of Rizatriptan Benzoate

NDC Code 0378-1404-05
Proprietary Name Rizatriptan Benzoate
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0378-1404-05)
Product NDC 0378-1404
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 Mylan Pharmaceuticals 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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