NDC 16714-757 – Atomoxetine

Atomoxetine Hydrochloride 25 mg/1 · Capsule · Oral

Human Prescription Drug 7 recalls

Product NDC16714-757

Product details

Brand name
Atomoxetine
Generic name
Atomoxetine
Labeler
Northstar Rx LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA079019
Marketed since
June 1, 2018
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
16714-757-0130 CAPSULE in 1 BOTTLE (16714-757-01)Jun 1, 2018

Recalls mentioning this NDC

Other Atomoxetine products