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Pseudoephedrine hydrochloride 30 MG Oral Capsule [Zephrex-D] — RxCUI 1918218

RxNorm drug concept · Semantic branded drug
RxCUI 1918218 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 2 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

RxCUI1918218
Official namePseudoephedrine hydrochloride 30 MG Oral Capsule [Zephrex-D]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asZephrex-D 30 MG Oral Capsule
FDA products mapped1
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

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

📗 Our plain-language guide HelloPharmacist
  • Pseudoephedrine is a decongestant — it works to temporarily shrink the swollen blood vessels inside your nasal passages and sinuses, which helps open things up so you can breathe m...
  • What exactly does pseudoephedrine do for my congestion?
  • Yes, it does. The regular tablets and Zephrex D capsules are taken every 4 to 6 hours, while extended-release tablets like Sudafed Sinus Congestion 12 Hour or Good Sense Suphedrine...
  • Does it matter which product or form I pick?
📖 Read our full Pseudoephedrine guide →

🕸️ Concept Web — How Pseudoephedrine hydrochloride 30 MG Oral Capsule... 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 Pseudoephedrine hydrochloride 30 MG Oral Capsule [Zephrex-D] RxCUI 1918218

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.

    • Pseudoephedrine 8896
    • Pseudoephedrine hydrochloride 91168
  2. Brand names 1

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

    • Zephrex-D 1358998
  3. Dose forms 13

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

    • Pseudoephedrine Oral Capsule 373667
    • Pseudoephedrine hydrochloride Oral Capsule 2647827
    • Pseudoephedrine Oral Product 1163567
    • Pseudoephedrine Pill 1163568
    • Pseudoephedrine hydrochloride Oral Product 2662900
    • Pseudoephedrine hydrochloride Pill 2662822
    • Pseudoephedrine Oral Capsule [Zephrex-D] 1918217
    • Pseudoephedrine hydrochloride Oral Capsule [Zephrex-D] 2655420
    • +5 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 — 14 of 19 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

  • Pseudoephedrine hydrochloride 30 MG Oral Capsule SCD · 1430169
  • Pseudoephedrine hydrochloride 30 MG SCDC · 996713
  • Pseudoephedrine Oral Capsule SCDF · 373667
  • Pseudoephedrine hydrochloride Oral Capsule SCDFP · 2647827
  • Pseudoephedrine Oral Product SCDG · 1163567
  • Pseudoephedrine Pill SCDG · 1163568
  • Pseudoephedrine hydrochloride Oral Product SCDGP · 2662900
  • Pseudoephedrine hydrochloride Pill SCDGP · 2662822

Brand-Name Concepts

  • Pseudoephedrine hydrochloride 30 MG [Zephrex-D] SBDC · 1358999
  • Pseudoephedrine Oral Capsule [Zephrex-D] SBDF · 1918217
  • Pseudoephedrine hydrochloride Oral Capsule [Zephrex-D] SBDFP · 2655420
  • Zephrex-D Oral Product SBDG · 1359001
  • Zephrex-D Pill SBDG · 1359002
  • Zephrex-D BN · 1358998

📦 FDA Products & Package NDCs

1 product · 2 package NDCs
2 package NDCs map to RxCUI 1918218 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
00113-0401-62 24 BLISTER PACK in 1 CARTON (0113-0401-62) / 1 CAPSULE, GEL... Zephrex D L. Perrigo Company 2017-04-17
00113-0401-67 48 BLISTER PACK in 1 CARTON (0113-0401-67) / 1 CAPSULE, GEL... Zephrex D L. Perrigo Company 2017-05-08
Observed labelers: L. Perrigo Company (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.