Atomoxetine

Product NDC
50090-6444
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atomoxetine
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA079016
Marketing category
ANDA
Substance
ATOMOXETINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6444-030 CAPSULE in 1 BOTTLE (50090-6444-0) 2023-04-19NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AtomoxetineA-S Medication Solutions2023-04-24Human Prescription Drug Label1