Paroxetine - 68084-044-01 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 68084-044
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: 68084-044
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20110519

Package Information of Paroxetine

Package NDC: 68084-044-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-044-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-044-11)

NDC Information of Paroxetine

NDC Code 68084-044-01
Proprietary Name Paroxetine
Package Description 10 BLISTER PACK in 1 CARTON (68084-044-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-044-11)
Product NDC 68084-044
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110519
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information