Home > National Drug Code (NDC) > Sertraline Hydrochloride

Sertraline Hydrochloride - 35356-668-30 - (Sertraline Hydrochloride)

Alphabetical Index


Drug Information of Sertraline Hydrochloride

Product NDC: 35356-668
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: 35356-668
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20071218

Package Information of Sertraline Hydrochloride

Package NDC: 35356-668-30
Package Description: 30 TABLET in 1 BOTTLE (35356-668-30)

NDC Information of Sertraline Hydrochloride

NDC Code 35356-668-30
Proprietary Name Sertraline Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (35356-668-30)
Product NDC 35356-668
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 Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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


General Information