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Quetiapine fumarate - 63629-4964-2 - (Quetiapine fumarate)

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Drug Information of Quetiapine fumarate

Product NDC: 63629-4964
Proprietary Name: Quetiapine fumarate
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 Quetiapine fumarate

Product NDC: 63629-4964
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202152
Marketing Category: ANDA
Start Marketing Date: 20120326

Package Information of Quetiapine fumarate

Package NDC: 63629-4964-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (63629-4964-2)

NDC Information of Quetiapine fumarate

NDC Code 63629-4964-2
Proprietary Name Quetiapine fumarate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (63629-4964-2)
Product NDC 63629-4964
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120326
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name QUETIAPINE FUMARATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine fumarate


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