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Sertraline hydrochloride - 13668-006-34 - (Sertraline hydrochloride)

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Drug Information of Sertraline hydrochloride

Product NDC: 13668-006
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: 13668-006
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077765
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Sertraline hydrochloride

Package NDC: 13668-006-34
Package Description: 2200 TABLET, FILM COATED in 1 BOTTLE (13668-006-34)

NDC Information of Sertraline hydrochloride

NDC Code 13668-006-34
Proprietary Name Sertraline hydrochloride
Package Description 2200 TABLET, FILM COATED in 1 BOTTLE (13668-006-34)
Product NDC 13668-006
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 Torrent Pharmaceuticals Limited
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


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