Mirtazapine

Product NDC
63629-9255
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076921
Marketing category
ANDA
Substance
MIRTAZAPINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-9255-130 TABLET, FILM COATED in 1 BOTTLE (63629-9255-1) 2022-04-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MirtazapineBryant Ranch Prepack2025-11-17HUMAN PRESCRIPTION DRUG LABEL103