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Fluoxetine

NDC 71335-0827 · Bryant Ranch Prepack

Generic nameFluoxetine Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)FLUOXETINE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

71335-0827-1 30 CAPSULE in 1 BOTTLE (71335-0827-1)

71335-0827-2 60 CAPSULE in 1 BOTTLE (71335-0827-2)

71335-0827-3 100 CAPSULE in 1 BOTTLE (71335-0827-3)

71335-0827-4 90 CAPSULE in 1 BOTTLE (71335-0827-4)

71335-0827-5 28 CAPSULE in 1 BOTTLE (71335-0827-5)

71335-0827-6 180 CAPSULE in 1 BOTTLE (71335-0827-6)

71335-0827-7 120 CAPSULE in 1 BOTTLE (71335-0827-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-125 — Fluoxetine Hydrochloride, 71205-178 — Fluoxetine, 71205-188 — Fluoxetine, 71205-393 — Fluoxetine Hydrochloride, 71205-974 — Fluoxetine Hydrochloride, 71205-975 — Fluoxetine Hydrochloride, 71205-979 — Fluoxetine Hydrochloride, 71209-040 — Fluoxetine, 71209-041 — Fluoxetine, 71209-042 — Fluoxetine, 71335-0923 — Fluoxetine Hydrochloride, 71335-0924 — Fluoxetine, 71335-1033 — Fluoxetine Hydrochloride, 71335-1048 — Fluoxetine, 71335-1145 — Fluoxetine Hydrochloride, 71335-1482 — Fluoxetine Hydrochloride, 71335-1548 — Fluoxetine Hydrochloride, 71335-2020 — Fluoxetine Hydrochloride, 71335-2597 — Fluoxetine, 71335-2778 — 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