Paroxetine - 54458-990-10 - (Paroxetine Hydrochloride)

Alphabetical Index


Drug Information of Paroxetine

Product NDC: 54458-990
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
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine

Product NDC: 54458-990
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20071211

Package Information of Paroxetine

Package NDC: 54458-990-10
Package Description: 30 TABLET in 1 BLISTER PACK (54458-990-10)

NDC Information of Paroxetine

NDC Code 54458-990-10
Proprietary Name Paroxetine
Package Description 30 TABLET in 1 BLISTER PACK (54458-990-10)
Product NDC 54458-990
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071211
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
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