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Sertraline Hydrochloride - 65862-011-99 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 65862-011
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: 65862-011
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077206
Marketing Category: ANDA
Start Marketing Date: 20070206

Package Information of Sertraline Hydrochloride

Package NDC: 65862-011-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-011-99)

NDC Information of Sertraline Hydrochloride

NDC Code 65862-011-99
Proprietary Name Sertraline Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-011-99)
Product NDC 65862-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070206
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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