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Quetiapine Fumarate - 0054-0220-25 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 0054-0220
Proprietary Name: Quetiapine Fumarate
Non Proprietary Name: Quetiapine Fumarate
Active Ingredient(s): 25    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: 0054-0220
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090749
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of Quetiapine Fumarate

Package NDC: 0054-0220-25
Package Description: 100 TABLET in 1 BOTTLE (0054-0220-25)

NDC Information of Quetiapine Fumarate

NDC Code 0054-0220-25
Proprietary Name Quetiapine Fumarate
Package Description 100 TABLET in 1 BOTTLE (0054-0220-25)
Product NDC 0054-0220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120327
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
Substance Name QUETIAPINE FUMARATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine Fumarate


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