NDC 50268-057 – Atomoxetine Hydrochloride

Atomoxetine Hydrochloride 25 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC50268-057

Product details

Brand name
Atomoxetine Hydrochloride
Generic name
Atomoxetine hydrochloride
Labeler
AvPAK
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078983
Marketed since
February 13, 2020
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
50268-057-1330 BLISTER PACK in 1 BOX (50268-057-13) / 1 CAPSULE in 1 BLISTER PACK (50268-057-11)Feb 13, 2020

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