NDC 68071-3284 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68071-3284

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 31, 2008
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (7)

Package NDCDescriptionSince
68071-3284-115 CAPSULE in 1 BOTTLE (68071-3284-1)May 23, 2017
68071-3284-220 CAPSULE in 1 BOTTLE (68071-3284-2)May 23, 2017
68071-3284-330 CAPSULE in 1 BOTTLE (68071-3284-3)May 23, 2017
68071-3284-556 CAPSULE in 1 BOTTLE (68071-3284-5)May 23, 2017
68071-3284-660 CAPSULE in 1 BOTTLE (68071-3284-6)May 23, 2017
68071-3284-828 CAPSULE in 1 BOTTLE (68071-3284-8)May 23, 2017
68071-3284-990 CAPSULE in 1 BOTTLE (68071-3284-9)May 23, 2017

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