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Quetiapine fumarate - 47335-903-61 - (Quetiapine fumarate)

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Drug Information of Quetiapine fumarate

Product NDC: 47335-903
Proprietary Name: Quetiapine fumarate
Non Proprietary Name: Quetiapine fumarate
Active Ingredient(s): 50    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: 47335-903
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: 47335-903-61
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-903-61) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Quetiapine fumarate

NDC Code 47335-903-61
Proprietary Name Quetiapine fumarate
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-903-61) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 47335-903
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 50
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine fumarate


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