NDC 23155-030 – Fluoxetine

Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC23155-030

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201336
Marketed since
October 13, 2024
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (4)

Package NDCDescriptionSince
23155-030-01100 CAPSULE in 1 BOTTLE (23155-030-01)Oct 13, 2024
23155-030-0330 CAPSULE in 1 BOTTLE (23155-030-03)Oct 13, 2024
23155-030-05500 CAPSULE in 1 BOTTLE (23155-030-05)Oct 13, 2024
23155-030-101000 CAPSULE in 1 BOTTLE (23155-030-10)Oct 13, 2024

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