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Rizatriptan Benzoate - 60505-3699-1 - (Rizatriptan Benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 60505-3699
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: 60505-3699
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202244
Marketing Category: ANDA
Start Marketing Date: 20121229

Package Information of Rizatriptan Benzoate

Package NDC: 60505-3699-1
Package Description: 3 BLISTER PACK in 1 CARTON (60505-3699-1) > 6 TABLET in 1 BLISTER PACK

NDC Information of Rizatriptan Benzoate

NDC Code 60505-3699-1
Proprietary Name Rizatriptan Benzoate
Package Description 3 BLISTER PACK in 1 CARTON (60505-3699-1) > 6 TABLET in 1 BLISTER PACK
Product NDC 60505-3699
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan Benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121229
Marketing Category Name ANDA
Labeler Name Apotex Corp
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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