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Quetiapine Fumarate - 0781-5342-13 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 0781-5342
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
Coding System: National Drug Codes(NDC)

Labeler Information of Quetiapine Fumarate

Product NDC: 0781-5342
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078679
Marketing Category: ANDA
Start Marketing Date: 20130405

Package Information of Quetiapine Fumarate

Package NDC: 0781-5342-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-5342-13) > 10 TABLET in 1 BLISTER PACK (0781-5342-06)

NDC Information of Quetiapine Fumarate

NDC Code 0781-5342-13
Proprietary Name Quetiapine Fumarate
Package Description 10 BLISTER PACK in 1 CARTON (0781-5342-13) > 10 TABLET in 1 BLISTER PACK (0781-5342-06)
Product NDC 0781-5342
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130405
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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