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Quetiapine Fumarate - 65862-493-10 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 65862-493
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: 65862-493
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091388
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of Quetiapine Fumarate

Package NDC: 65862-493-10
Package Description: 10 BLISTER PACK in 1 CARTON (65862-493-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Quetiapine Fumarate

NDC Code 65862-493-10
Proprietary Name Quetiapine Fumarate
Package Description 10 BLISTER PACK in 1 CARTON (65862-493-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 65862-493
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 Aurobindo Pharma Limited
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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