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Sertraline hydrochloride - 63629-3313-6 - (Sertraline hydrochloride)

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Drug Information of Sertraline hydrochloride

Product NDC: 63629-3313
Proprietary Name: Sertraline hydrochloride
Non Proprietary Name: Sertraline hydrochloride
Active Ingredient(s): 25    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: 63629-3313
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077765
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Sertraline hydrochloride

Package NDC: 63629-3313-6
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (63629-3313-6)

NDC Information of Sertraline hydrochloride

NDC Code 63629-3313-6
Proprietary Name Sertraline hydrochloride
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (63629-3313-6)
Product NDC 63629-3313
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070905
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Sertraline hydrochloride


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