NDC 60505-2835 – Atomoxetine Hydrochloride

Atomoxetine Hydrochloride 80 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC60505-2835

Product details

Brand name
Atomoxetine Hydrochloride
Generic name
Atomoxetine hydrochloride
Labeler
Apotex Corp.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078983
Marketed since
May 21, 2018
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
60505-2835-330 CAPSULE in 1 BOTTLE (60505-2835-3)May 21, 2018

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