Paroxetine - 59762-1812-3 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 59762-1812
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine Hydrochloride
Active Ingredient(s): 30    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: 59762-1812
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078406
Marketing Category: ANDA
Start Marketing Date: 20070725

Package Information of Paroxetine

Package NDC: 59762-1812-3
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (59762-1812-3)

NDC Information of Paroxetine

NDC Code 59762-1812-3
Proprietary Name Paroxetine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (59762-1812-3)
Product NDC 59762-1812
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070725
Marketing Category Name ANDA
Labeler Name Greenstone LLC
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information