PAXIL - 54868-2976-3 - (paroxetine hydrochloride)

Alphabetical Index


Drug Information of PAXIL

Product NDC: 54868-2976
Proprietary Name: PAXIL
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 PAXIL

Product NDC: 54868-2976
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020031
Marketing Category: NDA
Start Marketing Date: 20060918

Package Information of PAXIL

Package NDC: 54868-2976-3
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (54868-2976-3)

NDC Information of PAXIL

NDC Code 54868-2976-3
Proprietary Name PAXIL
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (54868-2976-3)
Product NDC 54868-2976
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name paroxetine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060918
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of PAXIL


General Information