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Naratriptan - 0378-4450-59 - (naratriptan)

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Drug Information of Naratriptan

Product NDC: 0378-4450
Proprietary Name: Naratriptan
Non Proprietary Name: naratriptan
Active Ingredient(s): 1    mg/1 & nbsp;   naratriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Naratriptan

Product NDC: 0378-4450
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202431
Marketing Category: ANDA
Start Marketing Date: 20120601

Package Information of Naratriptan

Package NDC: 0378-4450-59
Package Description: 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4450-59)

NDC Information of Naratriptan

NDC Code 0378-4450-59
Proprietary Name Naratriptan
Package Description 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4450-59)
Product NDC 0378-4450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naratriptan
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120601
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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