Quetiapine Fumarate

Product NDC
68788-7538
11-digit product format
687887538
Labeler code
68788
Product ID
68788-7538_87403a57-a481-4743-8d22-95204992ac40
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Quetiapine Fumarate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA202674
Marketing category
ANDA
Marketing start
2016-07-01
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
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7538-168788753801100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7538-1) 2019-12-270000-00-00NoNoCurrent
68788-7538-36878875380330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7538-3) 2019-12-270000-00-00NoNoCurrent
68788-7538-66878875380660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7538-6) 2019-12-270000-00-00NoNoCurrent
68788-7538-868788753808120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7538-8) 2019-12-270000-00-00NoNoCurrent
68788-7538-96878875380990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7538-9) 2019-12-270000-00-00NoNoCurrent