QUETIAPINE FUMARATE

Product NDC
13668-148
11-digit product format
136680148
Labeler code
13668
Product ID
13668-148_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
25 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
13668-148-01EA - Each13668-148759db9fe-899a-47a1-8b4b-26a45a4b9c0812012-07-24
13668-148-10EA - Each13668-1484d153dca-b641-4c47-9ddd-ac53eb5f22bd12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
13668-148-0113668014801100 TABLET in 1 BOTTLE (13668-148-01) 100 tablet2012-03-270000-00-00NoNoCurrent
13668-148-0513668014805500 TABLET in 1 BOTTLE (13668-148-05) 500 tablet2012-03-270000-00-00NoNoCurrent
13668-148-10136680148101000 TABLET in 1 BOTTLE (13668-148-10) 1000 tablet2012-03-270000-00-00NoNoCurrent
13668-148-301366801483030 TABLET in 1 BOTTLE (13668-148-30) 30 tablet2012-03-270000-00-00NoNoCurrent
13668-148-42136680148426000 TABLET in 1 BOTTLE (13668-148-42) 6000 tablet2012-03-270000-00-00NoNoCurrent
13668-148-7413668014874100 TABLET in 1 CARTON (13668-148-74) 100 tablet2012-03-270000-00-00NoNoCurrent