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SERTRALINE HYDROCHLORIDE - 52125-310-02 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 52125-310
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: 52125-310
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130513

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 52125-310-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-310-02)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 52125-310-02
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-310-02)
Product NDC 52125-310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SERTRALINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130513
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name REMEDYREPACK INC.
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


General Information