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Sertraline Hydrochloride - 65862-224-60 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 65862-224
Proprietary Name: Sertraline Hydrochloride
Non Proprietary Name: Sertraline Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Sertraline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Sertraline Hydrochloride

Product NDC: 65862-224
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078861
Marketing Category: ANDA
Start Marketing Date: 20081031

Package Information of Sertraline Hydrochloride

Package NDC: 65862-224-60
Package Description: 1 BOTTLE in 1 CARTON (65862-224-60) > 60 mL in 1 BOTTLE

NDC Information of Sertraline Hydrochloride

NDC Code 65862-224-60
Proprietary Name Sertraline Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (65862-224-60) > 60 mL in 1 BOTTLE
Product NDC 65862-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name SOLUTION, CONCENTRATE
Route Name ORAL
Start Marketing Date 20081031
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Sertraline Hydrochloride


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