QUETIAPINE FUMARATE

Product NDC
13668-149
11-digit product format
136680149
Labeler code
13668
Product ID
13668-149_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
50 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
13668-149-01EA - Each13668-149324bcdd3-0569-4b37-972e-6339d398902d12012-07-24
13668-149-10EA - Each13668-1491b58a2ed-565b-4ae2-b6b4-0736f191a02a12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
13668-149-0113668014901100 TABLET in 1 BOTTLE (13668-149-01) 100 tablet2012-03-270000-00-00NoNoCurrent
13668-149-0513668014905500 TABLET in 1 BOTTLE (13668-149-05) 500 tablet2012-03-270000-00-00NoNoCurrent
13668-149-10136680149101000 TABLET in 1 BOTTLE (13668-149-10) 1000 tablet2012-03-270000-00-00NoNoCurrent
13668-149-301366801493030 TABLET in 1 BOTTLE (13668-149-30) 30 tablet2012-03-270000-00-00NoNoCurrent
13668-149-58136680149584500 TABLET in 1 BOTTLE (13668-149-58) 4500 tablet2012-03-270000-00-00NoNoCurrent
13668-149-7413668014974100 TABLET in 1 CARTON (13668-149-74) 100 tablet2012-03-270000-00-00NoNoCurrent