SEROQUEL - 63629-3378-4 - (Quetiapine fumarate)

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Drug Information of SEROQUEL

Product NDC: 63629-3378
Proprietary Name: SEROQUEL
Non Proprietary Name: Quetiapine fumarate
Active Ingredient(s): 200    mg/1 & nbsp;   Quetiapine fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SEROQUEL

Product NDC: 63629-3378
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020639
Marketing Category: NDA
Start Marketing Date: 19971001

Package Information of SEROQUEL

Package NDC: 63629-3378-4
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE (63629-3378-4)

NDC Information of SEROQUEL

NDC Code 63629-3378-4
Proprietary Name SEROQUEL
Package Description 180 TABLET, FILM COATED in 1 BOTTLE (63629-3378-4)
Product NDC 63629-3378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19971001
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name QUETIAPINE FUMARATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of SEROQUEL


General Information