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Fluoxetine Hydrochloride

NDC 70954-600 · ANI Pharmaceuticals, Inc.

Generic nameFluoxetine Hydrochloride
Dosage formSOLUTION
RouteORAL
Active ingredient(s)FLUOXETINE HYDROCHLORIDE
Strength20 mg/5mL
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

70954-600-10 — 120 mL in 1 BOTTLE, PLASTIC (70954-600-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-1619 — Fluoxetine, 70518-3483 — Fluoxetine Hydrochloride, 70518-3554 — Fluoxetine Hydrochloride, 70518-3752 — Fluoxetine, 70518-4420 — Fluoxetine Hydrochloride, 70518-4428 — Fluoxetine, 70518-4429 — Fluoxetine, 70518-4543 — Fluoxetine, 70518-4576 — Fluoxetine, 70518-4611 — Fluoxetine, 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, +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