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Quetiapine fumarate - 47335-902-83 - (Quetiapine fumarate)

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Drug Information of Quetiapine fumarate

Product NDC: 47335-902
Proprietary Name: Quetiapine fumarate
Non Proprietary Name: Quetiapine fumarate
Active Ingredient(s): 25    mg/1 & nbsp;   Quetiapine fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quetiapine fumarate

Product NDC: 47335-902
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201190
Marketing Category: ANDA
Start Marketing Date: 20120328

Package Information of Quetiapine fumarate

Package NDC: 47335-902-83
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (47335-902-83)

NDC Information of Quetiapine fumarate

NDC Code 47335-902-83
Proprietary Name Quetiapine fumarate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (47335-902-83)
Product NDC 47335-902
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120328
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name QUETIAPINE FUMARATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine fumarate


General Information