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Sertraline Hydrochloride - 31722-213-05 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 31722-213
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: 31722-213
Labeler Name: Camber Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20071018

Package Information of Sertraline Hydrochloride

Package NDC: 31722-213-05
Package Description: 500 TABLET in 1 BOTTLE (31722-213-05)

NDC Information of Sertraline Hydrochloride

NDC Code 31722-213-05
Proprietary Name Sertraline Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (31722-213-05)
Product NDC 31722-213
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071018
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals Inc.
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