NDC 70518-0417 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-0417

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
April 10, 2017
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (3)

Package NDCDescriptionSince
70518-0417-130 CAPSULE in 1 BLISTER PACK (70518-0417-1)Apr 14, 2017
70518-0417-290 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-2)Apr 20, 2017
70518-0417-330 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-3)Apr 26, 2017

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