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Sennosides, USP 15 MG Oral Tablet — RxCUI 200162

RxNorm drug concept · Semantic clinical drug
RxCUI 200162 Semantic clinical drug · SCD ● Current RxNorm concept 7 FDA products 8 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

RxCUI200162
Official nameSennosides, USP 15 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known assennosides 15 MG Oral Tablet
FDA products mapped7
Package NDCs mapped8
Reported Medicaid activity (SDUD)192 prescriptions · 6 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

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🕸️ Concept Web — How Sennosides, USP 15 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 Sennosides, USP 15 MG Oral Tablet RxCUI 200162

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.

    • Sennosides, USP 36387
  2. Brand names 2

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

    • Ex-Lax Regular Strength Pills 217017
    • Perdiem Overnight 405262
  3. Dose forms 12

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

    • Sennosides, USP Oral Tablet 373859
    • Sennosides, USP Oral Product 1159068
    • Sennosides, USP Pill 1159069
    • Sennosides, USP Oral Tablet [Ex-Lax Regular Strength Pills] 368314
    • Sennosides, USP Oral Tablet [Perdiem Overnight] 406184
    • Ex-Lax Regular Strength Pills Oral Product 1171840
    • Ex-Lax Regular Strength Pills Pill 1171841
    • Perdiem Overnight Oral Product 1185809
    • +4 more in this family
  4. Clinical & branded drugs 5

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

Showing up to 8 concepts per family — 16 of 20 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

  • Sennosides, USP 15 MG SCDC · 331425
  • Sennosides, USP Oral Tablet SCDF · 373859
  • Sennosides, USP Oral Product SCDG · 1159068
  • Sennosides, USP Pill SCDG · 1159069

Brand-Name Concepts

  • Sennosides, USP 15 MG Oral Tablet [Ex-Lax Regular Strength Pills] SBD · 213072
  • Sennosides, USP 15 MG Oral Tablet [Perdiem Overnight] SBD · 404318
  • Sennosides, USP 15 MG [Ex-Lax Regular Strength Pills] SBDC · 573007
  • Sennosides, USP 15 MG [Perdiem Overnight] SBDC · 576309
  • Sennosides, USP Oral Tablet [Ex-Lax Regular Strength Pills] SBDF · 368314
  • Sennosides, USP Oral Tablet [Perdiem Overnight] SBDF · 406184
  • Ex-Lax Regular Strength Pills Oral Product SBDG · 1171840
  • Ex-Lax Regular Strength Pills Pill SBDG · 1171841
  • Perdiem Overnight Oral Product SBDG · 1185809
  • Perdiem Overnight Pill SBDG · 1185810

📦 FDA Products & Package NDCs

7 products · 8 package NDCs
8 package NDCs map to RxCUI 200162 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
00067-8141-01 1 BLISTER PACK in 1 CARTON (0067-8141-01) / 8 TABLET in 1 B... EX-LAX REGULAR STRENGTH STIMULANT LAXATIVE Haleon US Holdings LLC 2017-07-01
00067-8141-02 2 BLISTER PACK in 1 CARTON (0067-8141-02) / 15 TABLET in 1... EX-LAX REGULAR STRENGTH STIMULANT LAXATIVE Haleon US Holdings LLC 2017-07-01
00067-8143-01 1 BOTTLE in 1 CARTON (0067-8143-01) / 60 TABLET in 1 BOTTLE Perdiem Haleon US Holdings LLC 2017-07-01
37835-0214-45 3 BLISTER PACK in 1 CARTON (37835-214-45) / 15 TABLET, SUGA... Laxative Regular Strength Bi-Mart 2025-08-01
49483-0079-00 50000 TABLET, SUGAR COATED in 1 CARTON (49483-079-00) SENNOSIDES TIME CAP LABORATORIES, INC 2018-08-30
51316-0734-01 2 BLISTER PACK in 1 CARTON (51316-734-01) / 15 TABLET, SUGA... Stimulant Laxative CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED 2026-05-08
69842-0347-01 2 BLISTER PACK in 1 CARTON (69842-347-01) / 15 TABLET, SUGA... Laxative Regular Strength CVS PHARMACY 2003-12-08
70000-0443-01 2 BLISTER PACK in 1 CARTON (70000-0443-1) / 15 TABLET, SUGA... Laxative Cardinal Health 110, LLC. DBA Leader 2019-03-01
Observed labelers: Haleon US Holdings LLC (3) · Bi-Mart (1) · Cardinal Health 110, LLC. DBA Leader (1) · CVS PHARMACY (1) · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED (1) · TIME CAP LABORATORIES, INC (1) — 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.