NDC 70518-1619 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-1619

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076001
Marketed since
October 31, 2018
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-1619-230 CAPSULE in 1 BLISTER PACK (70518-1619-2)Jun 7, 2023

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