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Sertraline 50 MG Oral Tablet [Zoloft] — RxCUI 208161

RxNorm drug concept · Semantic branded drug
RxCUI 208161 Semantic branded drug · SBD ● Current RxNorm concept 4 FDA products 6 package NDCs Snapshot Jul 14, 2026

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

RxCUI208161
Official nameSertraline 50 MG Oral Tablet [Zoloft]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asZoloft 50 MG Oral Tablet; Zoloft (as sertraline hydrochloride) 50 MG Oral Tablet
FDA products mapped4
Package NDCs mapped6
Reported Medicaid activity (SDUD)1,908 prescriptions · 16 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 Sertraline: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It treats major depressive disorder and OCD. Many tablet and oral solution products also treat panic disorder, PTSD, social anxiety disorder, and PMDD. Capsules cover only depressi...
  • Take it by mouth, usually once a day, as your prescriber directs. The liquid must be diluted first, and capsules must be swallowed whole. Do not stop suddenly.
  • Nausea, loose stools, dry mouth, trouble sleeping, dizziness, sweating, and sexual side effects are common. Call your doctor if they bother you or don't ease.
  • Call if you have new or worse depression, suicidal thoughts, or unusual behavior changes. Also call for unusual bleeding, signs of serotonin syndrome, seizures, or eye pain.
📖 Read our full Sertraline guide →

🕸️ Concept Web — How Sertraline 50 MG Oral Tablet [Zoloft] 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 Sertraline 50 MG Oral Tablet [Zoloft] RxCUI 208161

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.

    • Sertraline 36437
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Zoloft 82728
  3. Dose forms 9

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

    • Sertraline Oral Tablet 373868
    • Sertraline Oral Product 1158194
    • Sertraline Pill 1158195
    • Sertraline Oral Tablet [Zoloft] 368413
    • Zoloft Oral Product 1188168
    • Zoloft Pill 1188169
    • Oral Tablet 317541
    • Oral Product 1151131
    • +1 more in this family
  4. Clinical & branded drugs 3

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

Showing up to 8 concepts per family — 13 of 14 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

  • Sertraline 50 MG Oral Tablet SCD · 312941
  • Sertraline 50 MG SCDC · 328671
  • Sertraline Oral Tablet SCDF · 373868
  • Sertraline Oral Product SCDG · 1158194
  • Sertraline Pill SCDG · 1158195

Brand-Name Concepts

  • Sertraline 50 MG [Zoloft] SBDC · 568885
  • Sertraline Oral Tablet [Zoloft] SBDF · 368413
  • Zoloft Oral Product SBDG · 1188168
  • Zoloft Pill SBDG · 1188169
  • Zoloft BN · 82728

📦 FDA Products & Package NDCs

4 products · 6 package NDCs
6 package NDCs map to RxCUI 208161 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
58151-0574-93 30 TABLET, FILM COATED in 1 BOTTLE (58151-574-93) Zoloft Viatris Specialty LLC 2024-10-30
58151-0575-88 100 BLISTER PACK in 1 CARTON (58151-575-88) / 1 TABLET, FIL... Zoloft Viatris Specialty LLC 2025-07-08
58151-0575-93 30 TABLET, FILM COATED in 1 BOTTLE (58151-575-93) Zoloft Viatris Specialty LLC 2025-07-08
58151-0576-88 100 BLISTER PACK in 1 CARTON (58151-576-88) / 1 TABLET, FIL... Zoloft Viatris Specialty LLC 2025-07-01
58151-0576-93 30 TABLET, FILM COATED in 1 BOTTLE (58151-576-93) Zoloft Viatris Specialty LLC 2024-11-26
58151-0601-35 1 BOTTLE, DROPPER in 1 CARTON (58151-601-35) / 60 mL in 1 B... Zoloft Viatris Specialty LLC 2024-11-21
Observed labelers: Viatris Specialty LLC (6) — 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.