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Fluoxetine

NDC 59651-324 · Aurobindo Pharma Limited

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

59651-324-30 — 30 TABLET, FILM COATED in 1 BOTTLE (59651-324-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-750 — Fluoxetine Hydrochloride, 51655-981 — Fluoxetine Hydrochloride, 51672-5306 — FLUOXETINE HYDROCHLORIDE, 53401-024 — Fluoxetine Hydrochloride, 54838-523 — Fluoxetine Hydrochloride, 55111-150 — Fluoxetine, 55111-284 — Fluoxetine Hydrochloride, 55154-2638 — Fluoxetine Hydrochloride, 59651-308 — Fluoxetine, 59651-309 — Fluoxetine, 59651-898 — Fluoxetine, 59651-899 — Fluoxetine, 59651-900 — Fluoxetine, 60687-659 — Fluoxetine Hydrochloride, 60687-845 — Fluoxetine, 60760-311 — Fluoxetine Hydrochloride, 62135-730 — Fluoxetine, 62332-022 — Fluoxetine, 62332-023 — Fluoxetine, 62332-024 — Fluoxetine, +221 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

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