QUETIAPINE FUMARATE

Product NDC
13668-150
11-digit product format
136680150
Labeler code
13668
Product ID
13668-150_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
100 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
13668-150-0113668015001100 TABLET in 1 BOTTLE (13668-150-01) 100 tablet2012-03-270000-00-00NoNoCurrent
13668-150-0513668015005500 TABLET in 1 BOTTLE (13668-150-05) 500 tablet2012-03-270000-00-00NoNoCurrent
13668-150-20136680150202000 TABLET in 1 BOTTLE (13668-150-20) 2000 tablet2012-03-270000-00-00NoNoCurrent
13668-150-301366801503030 TABLET in 1 BOTTLE (13668-150-30) 30 tablet2012-03-270000-00-00NoNoCurrent
13668-150-7413668015074100 TABLET in 1 CARTON (13668-150-74) 100 tablet2012-03-270000-00-00NoNoCurrent