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Quetiapine Fumarate - 0093-8163-10 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 0093-8163
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: 0093-8163
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077745
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of Quetiapine Fumarate

Package NDC: 0093-8163-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0093-8163-10)

NDC Information of Quetiapine Fumarate

NDC Code 0093-8163-10
Proprietary Name Quetiapine Fumarate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0093-8163-10)
Product NDC 0093-8163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine Fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120327
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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