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Naratriptan - 0054-0278-03 - (Naratriptan)

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Drug Information of Naratriptan

Product NDC: 0054-0278
Proprietary Name: Naratriptan
Non Proprietary Name: Naratriptan
Active Ingredient(s): 1    mg/1 & nbsp;   Naratriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naratriptan

Product NDC: 0054-0278
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090381
Marketing Category: ANDA
Start Marketing Date: 20100707

Package Information of Naratriptan

Package NDC: 0054-0278-03
Package Description: 9 TABLET in 1 BOTTLE (0054-0278-03)

NDC Information of Naratriptan

NDC Code 0054-0278-03
Proprietary Name Naratriptan
Package Description 9 TABLET in 1 BOTTLE (0054-0278-03)
Product NDC 0054-0278
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naratriptan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100707
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
Substance Name NARATRIPTAN HYDROCHLORIDE
Strength Number 1
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 Naratriptan


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