QUETIAPINE FUMARATE

Product NDC
13668-153
11-digit product format
136680153
Labeler code
13668
Product ID
13668-153_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
400 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
13668-153-0113668015301100 TABLET in 1 BOTTLE (13668-153-01) 100 tablet2012-03-270000-00-00NoNoCurrent
13668-153-0513668015305500 TABLET in 1 BOTTLE (13668-153-05) 500 tablet2012-03-270000-00-00NoNoCurrent
13668-153-20136680153202000 TABLET in 1 BOTTLE (13668-153-20) 2000 tablet2012-03-270000-00-00NoNoCurrent
13668-153-301366801533030 TABLET in 1 BOTTLE (13668-153-30) 30 tablet2012-03-270000-00-00NoNoCurrent
13668-153-7413668015374100 TABLET in 1 CARTON (13668-153-74) 100 tablet2012-03-270000-00-00NoNoCurrent