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Fluoxetine

NDC 72162-1506 · Bryant Ranch Prepack

Generic nameFluoxetine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FLUOXETINE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

72162-1506-3 — 30 TABLET, FILM COATED in 1 BOTTLE (72162-1506-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2020 — Fluoxetine Hydrochloride, 71335-2597 — Fluoxetine, 71335-2778 — Fluoxetine, 71335-2784 — Fluoxetine, 71335-2785 — fluoxetine, 71610-683 — Fluoxetine Hydrochloride, 71610-699 — Fluoxetine Hydrochloride, 71656-089 — FLUOXETINE, 72162-1494 — fluoxetine hydrochloride, 72162-1495 — fluoxetine hydrochloride, 72162-2221 — Fluoxetine Hydrochloride, 72189-067 — FLUOXETINE HYDROCHLORIDE, 72189-505 — Fluoxetine HCL, 72189-656 — Fluoxetine HCL, 72241-007 — Fluoxetine, 72241-008 — Fluoxetine, 72241-009 — Fluoxetine, 72603-488 — Fluoxetine, 72603-489 — Fluoxetine, 72603-490 — Fluoxetine, +221 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels