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SUMATRIPTAN - 54868-6052-0 - (sumatriptan)

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Drug Information of SUMATRIPTAN

Product NDC: 54868-6052
Proprietary Name: SUMATRIPTAN
Non Proprietary Name: sumatriptan
Active Ingredient(s): 20    mg/100uL & nbsp;   sumatriptan
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SUMATRIPTAN

Product NDC: 54868-6052
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020626
Marketing Category: NDA
Start Marketing Date: 20090723

Package Information of SUMATRIPTAN

Package NDC: 54868-6052-0
Package Description: 6 CONTAINER in 1 BOX (54868-6052-0) > 100 uL in 1 CONTAINER

NDC Information of SUMATRIPTAN

NDC Code 54868-6052-0
Proprietary Name SUMATRIPTAN
Package Description 6 CONTAINER in 1 BOX (54868-6052-0) > 100 uL in 1 CONTAINER
Product NDC 54868-6052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20090723
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name SUMATRIPTAN
Strength Number 20
Strength Unit mg/100uL
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of SUMATRIPTAN


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