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SERTRALINE HYDROCHLORIDE - 54868-5639-0 - (sertraline hydrochloride)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 54868-5639
Proprietary Name: SERTRALINE HYDROCHLORIDE
Non Proprietary Name: sertraline hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   sertraline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SERTRALINE HYDROCHLORIDE

Product NDC: 54868-5639
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20060824

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 54868-5639-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5639-0)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 54868-5639-0
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5639-0)
Product NDC 54868-5639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060824
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of SERTRALINE HYDROCHLORIDE


General Information