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Sertraline Hydrochloride - 54458-944-10 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 54458-944
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: 54458-944
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20090512

Package Information of Sertraline Hydrochloride

Package NDC: 54458-944-10
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (54458-944-10)

NDC Information of Sertraline Hydrochloride

NDC Code 54458-944-10
Proprietary Name Sertraline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (54458-944-10)
Product NDC 54458-944
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090512
Marketing Category Name ANDA
Labeler Name International Labs, 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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