SEROQUEL - 49349-902-02 - (Quetiapine fumarate)

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Drug Information of SEROQUEL

Product NDC: 49349-902
Proprietary Name: SEROQUEL
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 SEROQUEL

Product NDC: 49349-902
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020639
Marketing Category: NDA
Start Marketing Date: 20130509

Package Information of SEROQUEL

Package NDC: 49349-902-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-902-02)

NDC Information of SEROQUEL

NDC Code 49349-902-02
Proprietary Name SEROQUEL
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-902-02)
Product NDC 49349-902
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130509
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name QUETIAPINE FUMARATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of SEROQUEL


General Information