QUETIAPINE FUMARATE

Product NDC
13668-152
11-digit product format
136680152
Labeler code
13668
Product ID
13668-152_c0dfc06b-dbef-3d69-e053-2995a90aa31d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
QUETIAPINE FUMARATE
Dosage form
TABLET
Route
ORAL
Labeler
TORRENT PHARMACEUTICALS LIMITED
Application
ANDA200363
Marketing category
ANDA
Marketing start
2012-03-27
Marketing end
0000-00-00
Substance
QUETIAPINE FUMARATE
Active strength
300 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
13668-152-0113668015201100 TABLET in 1 BOTTLE (13668-152-01) 100 tablet2012-03-270000-00-00NoNoCurrent
13668-152-0513668015205500 TABLET in 1 BOTTLE (13668-152-05) 500 tablet2012-03-270000-00-00NoNoCurrent
13668-152-301366801523030 TABLET in 1 BOTTLE (13668-152-30) 30 tablet2012-03-270000-00-00NoNoCurrent
13668-152-31136680152312500 TABLET in 1 BOTTLE (13668-152-31) 2500 tablet2012-03-270000-00-00NoNoCurrent
13668-152-601366801526060 TABLET in 1 BOTTLE (13668-152-60) 60 tablet2012-03-270000-00-00NoNoCurrent
13668-152-7413668015274100 TABLET in 1 CARTON (13668-152-74) 100 tablet2012-03-270000-00-00NoNoCurrent