Paroxetine - 55154-6027-9 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 55154-6027
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: 55154-6027
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20070413

Package Information of Paroxetine

Package NDC: 55154-6027-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6027-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Paroxetine

NDC Code 55154-6027-9
Proprietary Name Paroxetine
Package Description 6 BLISTER PACK in 1 CARTON (55154-6027-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-6027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070413
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information