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PAROXETINE HYDROCHLORIDE - 63629-3327-2 - (paroxetine hydrochloride)

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Drug Information of PAROXETINE HYDROCHLORIDE

Product NDC: 63629-3327
Proprietary Name: PAROXETINE HYDROCHLORIDE
Non Proprietary Name: paroxetine hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   paroxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PAROXETINE HYDROCHLORIDE

Product NDC: 63629-3327
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020936
Marketing Category: NDA
Start Marketing Date: 20100913

Package Information of PAROXETINE HYDROCHLORIDE

Package NDC: 63629-3327-2
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3327-2)

NDC Information of PAROXETINE HYDROCHLORIDE

NDC Code 63629-3327-2
Proprietary Name PAROXETINE HYDROCHLORIDE
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3327-2)
Product NDC 63629-3327
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name paroxetine hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100913
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of PAROXETINE HYDROCHLORIDE


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