Home > National Drug Code (NDC) > Quetiapine Fumarate

Quetiapine Fumarate - 65862-491-99 - (Quetiapine Fumarate)

Alphabetical Index


Drug Information of Quetiapine Fumarate

Product NDC: 65862-491
Proprietary Name: Quetiapine Fumarate
Non Proprietary Name: Quetiapine Fumarate
Active Ingredient(s): 100    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: 65862-491
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: 65862-491-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-491-99)

NDC Information of Quetiapine Fumarate

NDC Code 65862-491-99
Proprietary Name Quetiapine Fumarate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-491-99)
Product NDC 65862-491
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 100
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine Fumarate


General Information