Quetiapine Fumarate

Product NDC
68071-1669
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Quetiapine Fumarate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA091388
Marketing category
ANDA
Substance
QUETIAPINE FUMARATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-1669-660 TABLET, FILM COATED in 1 BOTTLE (68071-1669-6) 2024-01-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Quetiapine FumarateNuCare Pharmaceuticals,Inc.2024-01-26HUMAN PRESCRIPTION DRUG LABEL1