NDC 71335-2162 – Atomoxetine

Atomoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2162

Product details

Brand name
Atomoxetine
Generic name
Atomoxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA079016
Marketed since
May 30, 2017
Listing expires
December 31, 2026
Pharmacologic class
Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Atomoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2162-130 CAPSULE in 1 BOTTLE (71335-2162-1)Sep 7, 2022

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