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QUETIAPINE FUMARATE - 13668-151-30 - (QUETIAPINE FUMARATE)

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Drug Information of QUETIAPINE FUMARATE

Product NDC: 13668-151
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
Coding System: National Drug Codes(NDC)

Labeler Information of QUETIAPINE FUMARATE

Product NDC: 13668-151
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200363
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of QUETIAPINE FUMARATE

Package NDC: 13668-151-30
Package Description: 30 TABLET in 1 BOTTLE (13668-151-30)

NDC Information of QUETIAPINE FUMARATE

NDC Code 13668-151-30
Proprietary Name QUETIAPINE FUMARATE
Package Description 30 TABLET in 1 BOTTLE (13668-151-30)
Product NDC 13668-151
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 Torrent Pharmaceuticals 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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