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Rizatriptan Benzoate - 49884-578-94 - (rizatriptan benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 49884-578
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: 49884-578
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020864
Marketing Category: NDA
Start Marketing Date: 19980629

Package Information of Rizatriptan Benzoate

Package NDC: 49884-578-94
Package Description: 18 POUCH in 1 CARTON (49884-578-94) > 1 TABLET in 1 POUCH (49884-578-52)

NDC Information of Rizatriptan Benzoate

NDC Code 49884-578-94
Proprietary Name Rizatriptan Benzoate
Package Description 18 POUCH in 1 CARTON (49884-578-94) > 1 TABLET in 1 POUCH (49884-578-52)
Product NDC 49884-578
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rizatriptan benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980629
Marketing Category Name NDA
Labeler Name Par Pharmaceutical 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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