NDC 68382-218 – Atomoxetine

Atomoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68382-218

Product details

Brand name
Atomoxetine
Generic name
Atomoxetine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA079017
Marketed since
June 12, 2017
Listing expires
December 31, 2026
Pharmacologic class
Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Atomoxetine →

Package NDC codes (6)

Package NDCDescriptionSince
68382-218-022000 CAPSULE in 1 BOTTLE (68382-218-02)Jun 12, 2017
68382-218-0630 CAPSULE in 1 BOTTLE (68382-218-06)Jun 12, 2017
68382-218-101000 CAPSULE in 1 BOTTLE (68382-218-10)Jun 12, 2017
68382-218-1460 CAPSULE in 1 BOTTLE (68382-218-14)Jun 12, 2017
68382-218-1690 CAPSULE in 1 BOTTLE (68382-218-16)Jun 12, 2017
68382-218-7710 BLISTER PACK in 1 CARTON (68382-218-77) / 10 CAPSULE in 1 BLISTER PACK (68382-218-30)Jun 12, 2017

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