Home > National Drug Code (NDC) > Sertraline Hydrochloride

Sertraline Hydrochloride - 24236-633-38 - (sertraline hydrochloride)

Alphabetical Index


Drug Information of Sertraline Hydrochloride

Product NDC: 24236-633
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: 24236-633
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077864
Marketing Category: ANDA
Start Marketing Date: 20130228

Package Information of Sertraline Hydrochloride

Package NDC: 24236-633-38
Package Description: 3 TABLET, FILM COATED in 1 BLISTER PACK (24236-633-38)

NDC Information of Sertraline Hydrochloride

NDC Code 24236-633-38
Proprietary Name Sertraline Hydrochloride
Package Description 3 TABLET, FILM COATED in 1 BLISTER PACK (24236-633-38)
Product NDC 24236-633
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130228
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


General Information