NDC 70518-4313 – Atomoxetine Hydrochloride

Atomoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-4313

Product details

Brand name
Atomoxetine Hydrochloride
Generic name
Atomoxetine hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078983
Marketed since
March 19, 2025
Listing expires
December 31, 2027
Pharmacologic class
Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Atomoxetine hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4313-030 POUCH in 1 BOX (70518-4313-0) / 1 CAPSULE in 1 POUCH (70518-4313-1)Mar 19, 2025

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