Paroxetine - 0615-5576-05 - (Paroxetine)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 0615-5576
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Paroxetine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine

Product NDC: 0615-5576
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20070307

Package Information of Paroxetine

Package NDC: 0615-5576-05
Package Description: 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-5576-05)

NDC Information of Paroxetine

NDC Code 0615-5576-05
Proprietary Name Paroxetine
Package Description 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-5576-05)
Product NDC 0615-5576
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070307
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PAROXETINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information