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SERTRALINE HYDROCHLORIDE - 54868-5638-6 - (sertraline hydrochloride)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 54868-5638
Proprietary Name: SERTRALINE HYDROCHLORIDE
Non Proprietary Name: sertraline hydrochloride
Active Ingredient(s): 100    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: 54868-5638
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20060912

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 54868-5638-6
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (54868-5638-6)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 54868-5638-6
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (54868-5638-6)
Product NDC 54868-5638
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060912
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of SERTRALINE HYDROCHLORIDE


General Information