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Naratriptan - 23155-054-19 - (Naratriptan)

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Drug Information of Naratriptan

Product NDC: 23155-054
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: 23155-054
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200502
Marketing Category: ANDA
Start Marketing Date: 20110315

Package Information of Naratriptan

Package NDC: 23155-054-19
Package Description: 9 TABLET in 1 BLISTER PACK (23155-054-19)

NDC Information of Naratriptan

NDC Code 23155-054-19
Proprietary Name Naratriptan
Package Description 9 TABLET in 1 BLISTER PACK (23155-054-19)
Product NDC 23155-054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naratriptan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110315
Marketing Category Name ANDA
Labeler Name Heritage 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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