Paroxetine - 67046-531-30 - (Paroxetine hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 67046-531
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: 67046-531
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20100811

Package Information of Paroxetine

Package NDC: 67046-531-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-531-30)

NDC Information of Paroxetine

NDC Code 67046-531-30
Proprietary Name Paroxetine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-531-30)
Product NDC 67046-531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100811
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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