Paroxetine - 0093-7121-98 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 0093-7121
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine Hydrochloride
Active Ingredient(s): 40    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: 0093-7121
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076618
Marketing Category: ANDA
Start Marketing Date: 20051102

Package Information of Paroxetine

Package NDC: 0093-7121-98
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0093-7121-98)

NDC Information of Paroxetine

NDC Code 0093-7121-98
Proprietary Name Paroxetine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0093-7121-98)
Product NDC 0093-7121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051102
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PAROXETINE HYDROCHLORIDE ANHYDROUS
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information