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Fluoxetine

NDC 77771-113 · RADHA PHARMACEUTICALS, INC.

Generic nameFluoxetine Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)FLUOXETINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

77771-113-01 — 100 CAPSULE in 1 BOTTLE (77771-113-01)

77771-113-10 — 1000 CAPSULE in 1 BOTTLE (77771-113-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72241-007 — Fluoxetine, 72241-008 — Fluoxetine, 72241-009 — Fluoxetine, 72603-488 — Fluoxetine, 72603-489 — Fluoxetine, 72603-490 — Fluoxetine, 72789-545 — Fluoxetine Hydrochloride, 72789-554 — Fluoxetine, 72789-557 — Fluoxetine, 75834-148 — fluoxetine hydrochloride, 77771-114 — Fluoxetine Hydrochloride, 77771-115 — Fluoxetine Hydrochloride, 80425-0313 — Fluoxetine, 82009-100 — Fluoxetine Hydrochloride, 82009-101 — Fluoxetine Hydrochloride, 82009-102 — Fluoxetine Hydrochloride, 82868-098 — Fluoxetine, 82868-105 — Fluoxetine, 83209-192 — Fluoxetine Hydrochloride, 83209-721 — 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