NDC 63629-8989 – Fluoxetine hydrochloride

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

Human Prescription Drug

Product NDC63629-8989

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, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
63629-8989-160 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-8989-1)Dec 7, 2021
63629-8989-290 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-8989-2)Dec 7, 2021

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