NDC 71610-699 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71610-699

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204597
Marketed since
October 24, 2022
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (6)

Package NDCDescriptionSince
71610-699-3030 CAPSULE in 1 BOTTLE (71610-699-30)Apr 3, 2023
71610-699-5360 CAPSULE in 1 BOTTLE (71610-699-53)Apr 3, 2023
71610-699-6090 CAPSULE in 1 BOTTLE (71610-699-60)Apr 3, 2023
71610-699-70120 CAPSULE in 1 BOTTLE (71610-699-70)Apr 3, 2023
71610-699-80180 CAPSULE in 1 BOTTLE (71610-699-80)Apr 3, 2023
71610-699-92270 CAPSULE in 1 BOTTLE (71610-699-92)Apr 3, 2023

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