NDC 68071-4033 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68071-4033

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076001
Marketed since
January 29, 2002
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
68071-4033-115 CAPSULE in 1 BOTTLE (68071-4033-1)Aug 7, 2017
68071-4033-220 CAPSULE in 1 BOTTLE (68071-4033-2)Aug 7, 2017
68071-4033-330 CAPSULE in 1 BOTTLE (68071-4033-3)Aug 7, 2017
68071-4033-556 CAPSULE in 1 BOTTLE (68071-4033-5)Aug 7, 2017
68071-4033-660 CAPSULE in 1 BOTTLE (68071-4033-6)Aug 7, 2017
68071-4033-828 CAPSULE in 1 BOTTLE (68071-4033-8)Aug 7, 2017
68071-4033-990 CAPSULE in 1 BOTTLE (68071-4033-9)Aug 7, 2017

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