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Sertraline Hydrochloride - 55154-1026-9 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 55154-1026
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
Coding System: National Drug Codes(NDC)

Labeler Information of Sertraline Hydrochloride

Product NDC: 55154-1026
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20071218

Package Information of Sertraline Hydrochloride

Package NDC: 55154-1026-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-1026-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Sertraline Hydrochloride

NDC Code 55154-1026-9
Proprietary Name Sertraline Hydrochloride
Package Description 6 BLISTER PACK in 1 CARTON (55154-1026-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-1026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071218
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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