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Sertraline Hydrochloride - 24236-729-27 - (sertraline hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 24236-729
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: 24236-729
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077864
Marketing Category: ANDA
Start Marketing Date: 20130328

Package Information of Sertraline Hydrochloride

Package NDC: 24236-729-27
Package Description: 270 TABLET, FILM COATED in 1 CANISTER (24236-729-27)

NDC Information of Sertraline Hydrochloride

NDC Code 24236-729-27
Proprietary Name Sertraline Hydrochloride
Package Description 270 TABLET, FILM COATED in 1 CANISTER (24236-729-27)
Product NDC 24236-729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130328
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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