NDC 23155-028 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC23155-028

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 (2)

Package NDCDescriptionSince
23155-028-01100 CAPSULE in 1 BOTTLE (23155-028-01)Oct 13, 2024
23155-028-101000 CAPSULE in 1 BOTTLE (23155-028-10)Oct 13, 2024

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