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Protriptyline hydrochloride 10 MG Oral Tablet — RxCUI 905168

RxNorm drug concept · Semantic clinical drug
RxCUI 905168 Semantic clinical drug · SCD ● Current RxNorm concept 4 FDA products 8 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

RxCUI905168
Official nameProtriptyline hydrochloride 10 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asprotriptyline HCl 10 MG Oral Tablet
FDA products mapped4
Package NDCs mapped8
Reported Medicaid activity (SDUD)729 prescriptions · 6 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 Protriptyline: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It treats symptoms of depression in people who are under close medical supervision. It has an activating effect, so it can suit people who feel withdrawn and low on energy.
  • It's taken by mouth, usually split into 3 or 4 doses a day. Your prescriber will start low and increase slowly, with any increases in the morning dose. Follow your label exactly an...
  • Dry mouth, constipation, blurred vision, dizziness, fast heartbeat and feeling jittery or anxious are among the possibilities. Let your prescriber know if they bother you, since a...
  • Call if your mood worsens, you have thoughts of suicide, or you notice unusual behavior changes. Also get help for chest pain, stroke symptoms, seizures, hallucinations, rash or sw...
📖 Read our full Protriptyline guide →

🕸️ Concept Web — How Protriptyline hydrochloride 10 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 Protriptyline hydrochloride 10 MG Oral Tablet RxCUI 905168

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

  1. Ingredients 2

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

    • Protriptyline 8886
    • Protriptyline hydrochloride 203199
  2. Dose forms 9

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

    • Protriptyline Oral Tablet 373665
    • Protriptyline hydrochloride Oral Tablet 2647871
    • Protriptyline Oral Product 1162958
    • Protriptyline Pill 1162959
    • Protriptyline hydrochloride Oral Product 2660713
    • Protriptyline hydrochloride Pill 2659753
    • Oral Tablet 317541
    • Oral Product 1151131
    • +1 more in this family
  3. Clinical & branded drugs 1

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

    • Protriptyline hydrochloride 10 MG 905167

Showing up to 8 concepts per family — 11 of 12 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

  • Protriptyline hydrochloride 10 MG SCDC · 905167
  • Protriptyline Oral Tablet SCDF · 373665
  • Protriptyline hydrochloride Oral Tablet SCDFP · 2647871
  • Protriptyline Oral Product SCDG · 1162958
  • Protriptyline Pill SCDG · 1162959
  • Protriptyline hydrochloride Oral Product SCDGP · 2660713
  • Protriptyline hydrochloride Pill SCDGP · 2659753

📦 FDA Products & Package NDCs

4 products · 8 package NDCs
8 package NDCs map to RxCUI 905168 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
42794-0004-02 100 TABLET, FILM COATED in 1 BOTTLE (42794-004-02) Protriptyline Hydrochloride Sigmapharm Laboratories, LLC 2020-03-02
42794-0007-02 100 TABLET, FILM COATED in 1 BOTTLE (42794-007-02) Protriptyline Hydrochloride Sigmapharm Laboratories, LLC 2020-03-02
42806-0096-01 100 TABLET, FILM COATED in 1 BOTTLE (42806-096-01) Protriptyline Hydrochloride Epic Pharma, LLC 2013-01-09
42806-0096-10 1000 TABLET, FILM COATED in 1 BOTTLE (42806-096-10) Protriptyline Hydrochloride Epic Pharma, LLC 2013-01-09
42806-0096-30 30 TABLET, FILM COATED in 1 BOTTLE (42806-096-30) Protriptyline Hydrochloride Epic Pharma, LLC 2020-07-10
42806-0097-01 100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01) Protriptyline Hydrochloride Epic Pharma, LLC 2013-01-09
42806-0097-10 1000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10) Protriptyline Hydrochloride Epic Pharma, LLC 2013-01-09
42806-0097-30 30 TABLET, FILM COATED in 1 BOTTLE (42806-097-30) Protriptyline Hydrochloride Epic Pharma, LLC 2020-07-10
Observed labelers: Epic Pharma, LLC (6) · Sigmapharm Laboratories, LLC (2) — 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.