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Paroxetine Hydrochloride - 54868-6178-0 - (paroxetine hydrochloride)

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Drug Information of Paroxetine Hydrochloride

Product NDC: 54868-6178
Proprietary Name: Paroxetine Hydrochloride
Non Proprietary Name: paroxetine hydrochloride
Active Ingredient(s): 12.5    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: 54868-6178
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077873
Marketing Category: ANDA
Start Marketing Date: 20101025

Package Information of Paroxetine Hydrochloride

Package NDC: 54868-6178-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-6178-0)

NDC Information of Paroxetine Hydrochloride

NDC Code 54868-6178-0
Proprietary Name Paroxetine Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-6178-0)
Product NDC 54868-6178
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 20101025
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine Hydrochloride


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