PAROXETINE - 54868-4937-3 - (paroxetine hydrochloride)

Alphabetical Index


Drug Information of PAROXETINE

Product NDC: 54868-4937
Proprietary Name: PAROXETINE
Non Proprietary Name: paroxetine hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   paroxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of PAROXETINE

Product NDC: 54868-4937
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075356
Marketing Category: ANDA
Start Marketing Date: 20081015

Package Information of PAROXETINE

Package NDC: 54868-4937-3
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (54868-4937-3)

NDC Information of PAROXETINE

NDC Code 54868-4937-3
Proprietary Name PAROXETINE
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (54868-4937-3)
Product NDC 54868-4937
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name paroxetine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081015
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PAROXETINE HYDROCHLORIDE ANHYDROUS
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of PAROXETINE


General Information