NDC 72162-1494 – Fluoxetine hydrochloride

Fluoxetine Hydrochloride 10 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC72162-1494

Product details

Brand name
Fluoxetine hydrochloride
Generic name
Fluoxetine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA203836
Marketed since
August 22, 2016
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
72162-1494-1100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-1)Oct 4, 2023
72162-1494-330 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-3)Oct 4, 2023

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