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Sertraline Hydrochloride - 63304-168-10 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 63304-168
Proprietary Name: Sertraline Hydrochloride
Non Proprietary Name: Sertraline Hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Sertraline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sertraline Hydrochloride

Product NDC: 63304-168
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077977
Marketing Category: ANDA
Start Marketing Date: 20070206

Package Information of Sertraline Hydrochloride

Package NDC: 63304-168-10
Package Description: 1000 TABLET, COATED in 1 BOTTLE (63304-168-10)

NDC Information of Sertraline Hydrochloride

NDC Code 63304-168-10
Proprietary Name Sertraline Hydrochloride
Package Description 1000 TABLET, COATED in 1 BOTTLE (63304-168-10)
Product NDC 63304-168
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20070206
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Sertraline Hydrochloride


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