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Fluoxetine 60 MG Oral Tablet — RxCUI 1190110

RxNorm drug concept · Semantic clinical drug
RxCUI 1190110 Semantic clinical drug · SCD ● Current RxNorm concept 14 FDA products 18 package NDCs Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI1190110
Official nameFluoxetine 60 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asfluoxetine (as fluoxetine HCl) 60 MG Oral Tablet; FLUoxetine HCl 60 MG Oral Tablet
FDA products mapped14
Package NDCs mapped18
Reported Medicaid activity (SDUD)128,466 prescriptions · 48 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Fluoxetine: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Fluoxetine is an SSRI antidepressant. Most products treat major depressive disorder, OCD, bulimia nervosa and panic disorder. Some products, like the delayed-release capsules, are...
  • Take it by mouth, usually once a day in the morning, with or without food. Follow the directions on your label. Don't stop suddenly without talking to your prescriber.
  • Common ones are nausea, headache, trouble sleeping, nervousness, diarrhea, dry mouth, sleepiness and sweating. Sexual side effects can also happen. Call your doctor if they bother...
  • Call for new or worse depression, suicidal thoughts, agitation or unusual behavior changes, especially early on or after dose changes. Also get help for a rash, unusual bleeding, f...
📖 Read our full Fluoxetine guide →

🕸️ Concept Web — How Fluoxetine 60 MG Oral Tablet Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Fluoxetine 60 MG Oral Tablet RxCUI 1190110

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 1

    The active substance itself — no strength, form, or brand attached yet.

    • Fluoxetine 4493
  2. Dose forms 6

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Fluoxetine Oral Tablet 372233
    • Fluoxetine Oral Product 1160836
    • Fluoxetine Pill 1160837
    • Oral Tablet 317541
    • Oral Product 1151131
    • Pill 1151133
  3. Clinical & branded drugs 1

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

    • Fluoxetine 60 MG 334800

Showing up to 8 concepts per family — 8 of 8 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Fluoxetine 60 MG SCDC · 334800
  • Fluoxetine Oral Tablet SCDF · 372233
  • Fluoxetine Oral Product SCDG · 1160836
  • Fluoxetine Pill SCDG · 1160837

📦 FDA Products & Package NDCs

14 products · 18 package NDCs
18 package NDCs map to RxCUI 1190110 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
16714-0114-01 30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01) Fluoxetine hydrochloride NorthStar Rx LLC 2019-09-18
43598-0632-01 100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01) Fluoxetine hydrochloride Dr. Reddy's Laboratories Inc. 2019-01-28
43598-0632-30 30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30) Fluoxetine hydrochloride Dr. Reddy's Laboratories Inc. 2019-01-28
49884-0468-11 30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11) Fluoxetine Par Health USA, LLC 2017-11-16
50228-0422-10 1000 TABLET in 1 BOTTLE (50228-422-10) Fluoxetine ScieGen Pharmaceuticals, Inc. 2019-01-10
50228-0422-30 30 TABLET in 1 BOTTLE (50228-422-30) Fluoxetine ScieGen Pharmaceuticals, Inc. 2019-01-10
50228-0638-10 1000 TABLET in 1 BOTTLE (50228-638-10) Fluoxetine ScieGen Pharmaceuticals, Inc. 2025-09-11
50228-0638-30 30 TABLET in 1 BOTTLE (50228-638-30) Fluoxetine ScieGen Pharmaceuticals, Inc. 2025-09-11
51672-5306-02 500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2) FLUOXETINE HYDROCHLORIDE Taro Pharmaceuticals U.S.A., Inc. 2019-02-15
51672-5306-06 30 TABLET, FILM COATED in 1 BOTTLE (51672-5306-6) FLUOXETINE HYDROCHLORIDE Taro Pharmaceuticals U.S.A., Inc. 2019-02-15
59651-0324-30 30 TABLET, FILM COATED in 1 BOTTLE (59651-324-30) Fluoxetine Aurobindo Pharma Limited 2020-06-10
63629-2201-01 30 TABLET, FILM COATED in 1 BOTTLE (63629-2201-1) Fluoxetine Bryant Ranch Prepack 2022-10-28
64380-0900-04 30 TABLET in 1 BOTTLE (64380-900-04) FLUOXETINE HCL Strides Pharma Science Limited 2024-11-08
68180-0997-06 30 TABLET in 1 BOTTLE (68180-997-06) Fluoxetine Hydrochloride Lupin Pharmaceuticals, Inc. 2019-04-09
71335-2597-01 30 TABLET, FILM COATED in 1 BOTTLE (71335-2597-1) Fluoxetine Bryant Ranch Prepack 2025-02-12
72162-1506-03 30 TABLET, FILM COATED in 1 BOTTLE (72162-1506-3) Fluoxetine Bryant Ranch Prepack 2024-04-08
75834-0148-30 30 TABLET in 1 BOTTLE (75834-148-30) fluoxetine NIVAGEN PHARMACEUTICALS, INC. 2017-12-11
84386-0106-30 30 TABLET, FILM COATED in 1 BOTTLE (84386-106-30) Fluoxetine Aurobindo Pharma Limited 2026-01-15
Observed labelers: ScieGen Pharmaceuticals, Inc. (4) · Bryant Ranch Prepack (3) · Aurobindo Pharma Limited (2) · Dr. Reddy's Laboratories Inc. (2) · Taro Pharmaceuticals U.S.A., Inc. (2) · Lupin Pharmaceuticals, Inc. (1) · +4 more — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.