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Sertraline Hydrochloride - 68180-351-08 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 68180-351
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: 68180-351
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077670
Marketing Category: ANDA
Start Marketing Date: 20070201

Package Information of Sertraline Hydrochloride

Package NDC: 68180-351-08
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (68180-351-08)

NDC Information of Sertraline Hydrochloride

NDC Code 68180-351-08
Proprietary Name Sertraline Hydrochloride
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (68180-351-08)
Product NDC 68180-351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070201
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
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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