Paroxetine - 52125-360-02 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 52125-360
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine Hydrochloride
Active Ingredient(s): 10    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: 52125-360
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20130604

Package Information of Paroxetine

Package NDC: 52125-360-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-360-02)

NDC Information of Paroxetine

NDC Code 52125-360-02
Proprietary Name Paroxetine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-360-02)
Product NDC 52125-360
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130604
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PAROXETINE HYDROCHLORIDE ANHYDROUS
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information