Paroxetine - 65841-097-16 - (Paroxetine Hydrochloride)

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Drug Information of Paroxetine

Product NDC: 65841-097
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: 65841-097
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20070413

Package Information of Paroxetine

Package NDC: 65841-097-16
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (65841-097-16)

NDC Information of Paroxetine

NDC Code 65841-097-16
Proprietary Name Paroxetine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (65841-097-16)
Product NDC 65841-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070413
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information