NDC 0093-3547 – Atomoxetine

Atomoxetine Hydrochloride 80 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0093-3547

Product details

Brand name
Atomoxetine
Generic name
Atomoxetine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA079022
Marketed since
May 30, 2017
Listing expires
December 31, 2027
Pharmacologic class
Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Atomoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
0093-3547-5630 CAPSULE in 1 BOTTLE (0093-3547-56)May 30, 2017

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