Paroxetine - 68382-097-16 - (Paroxetine)

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Drug Information of Paroxetine

Product NDC: 68382-097
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Paroxetine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine

Product NDC: 68382-097
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20070413

Package Information of Paroxetine

Package NDC: 68382-097-16
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16)

NDC Information of Paroxetine

NDC Code 68382-097-16
Proprietary Name Paroxetine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16)
Product NDC 68382-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070413
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
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