Paroxetine - 13107-155-99 - (Paroxetine)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 13107-155
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine
Active Ingredient(s): 20    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: 13107-155
Labeler Name: Aurolife Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078406
Marketing Category: ANDA
Start Marketing Date: 20091203

Package Information of Paroxetine

Package NDC: 13107-155-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (13107-155-99)

NDC Information of Paroxetine

NDC Code 13107-155-99
Proprietary Name Paroxetine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (13107-155-99)
Product NDC 13107-155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091203
Marketing Category Name ANDA
Labeler Name Aurolife Pharma LLC
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information