PAXIL - 60505-3669-3 - (paroxetine hydrochloride)

Alphabetical Index


Drug Information of PAXIL

Product NDC: 60505-3669
Proprietary Name: PAXIL
Non Proprietary Name: paroxetine hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   paroxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PAXIL

Product NDC: 60505-3669
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020936
Marketing Category: NDA
Start Marketing Date: 20110101

Package Information of PAXIL

Package NDC: 60505-3669-3
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3669-3)

NDC Information of PAXIL

NDC Code 60505-3669-3
Proprietary Name PAXIL
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3669-3)
Product NDC 60505-3669
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name paroxetine hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name NDA
Labeler Name Apotex Corp
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of PAXIL


General Information