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Meclizine hydrochloride 25 MG Oral Tablet [Dramamine Nausea Relief] — RxCUI 2110527

Name: Meclizine hydrochloride 25 MG Oral Tablet [Dramamine Nausea Relief] (RxCUI 2110527)
Creator: Brian Staiger, PharmD

RxNorm drug concept · Semantic branded drug

RxCUI 2110527 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 1 package NDC Snapshot Jul 14, 2026

This page is curated, coded, and maintained by Dr. Brian Staiger, PharmD

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

RxCUI2110527

Official nameMeclizine hydrochloride 25 MG Oral Tablet [Dramamine Nausea Relief]

Concept typeSemantic branded drug (SBD)

RxNorm statusCurrent RxNorm concept

Also known asDramamine Nausea Relief 25 MG Oral Tablet

FDA products mapped1

Package NDCs mapped1

RxNorm release07/06/2026

Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

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

📗 Our plain-language guide HelloPharmacist

Meclizine is mainly used to prevent and treat the nausea, vomiting, and dizziness that comes with motion sickness — whether you're on a boat, in a car, or on a plane. It's also use...
For the best chance of preventing motion sickness, take meclizine about one hour before you start traveling. After that first dose, you can take it once every 24 hours as needed fo...
Yes, drowsiness is the most common side effect — it's actually worth planning around. Avoid driving or operating heavy machinery until you know how it affects you. And definitely s...
This one requires a conversation with your doctor. Human studies haven't clearly linked meclizine to birth defects, but animal studies did show fetal harm at doses similar to what...

📖 Read our full Meclizine guide →

🕸️ Concept Web — How Meclizine hydrochloride 25 MG Oral Tablet [Drama... 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 Meclizine hydrochloride 25 MG Oral Tablet [Dramamine Nausea Relief] RxCUI 2110527 Semantic branded drug · SBD

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

Ingredients 2

The active substance itself — no strength, form, or brand attached yet.
- Meclizine 6676 IN
- Meclizine hydrochloride 82041 PIN
Brand names 1

The same medicine's trade names. A brand name alone says nothing about strength or form.
- Dramamine Nausea Relief 2110522 BN
Dose forms 13

The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
- Meclizine Oral Tablet 372731 SCDF
- Meclizine hydrochloride Oral Tablet 2645970 SCDFP
- Meclizine Oral Product 1159177 SCDG
- Meclizine Pill 1159178 SCDG
- Meclizine hydrochloride Oral Product 2659152 SCDGP
- Meclizine hydrochloride Pill 2660116 SCDGP
- Meclizine Oral Tablet [Dramamine Nausea Relief] 2110524 SBDF
- Meclizine hydrochloride Oral Tablet [Dramamine Nausea Relief] 2657551 SBDFP
- +5 more in this family
Clinical & branded drugs 3

Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
- Meclizine hydrochloride 25 MG Oral Tablet 995666 SCD
- Meclizine hydrochloride 25 MG 995631 SCDC
- Meclizine hydrochloride 25 MG [Dramamine Nausea Relief] 2110523 SBDC

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

Meclizine hydrochloride 25 MG Oral Tablet SCD · 995666
Meclizine hydrochloride 25 MG SCDC · 995631
Meclizine Oral Tablet SCDF · 372731
Meclizine hydrochloride Oral Tablet SCDFP · 2645970
Meclizine Oral Product SCDG · 1159177
Meclizine Pill SCDG · 1159178
Meclizine hydrochloride Oral Product SCDGP · 2659152
Meclizine hydrochloride Pill SCDGP · 2660116

Brand-Name Concepts

Meclizine hydrochloride 25 MG [Dramamine Nausea Relief] SBDC · 2110523
Meclizine Oral Tablet [Dramamine Nausea Relief] SBDF · 2110524
Meclizine hydrochloride Oral Tablet [Dramamine Nausea Relief] SBDFP · 2657551
Dramamine Nausea Relief Oral Product SBDG · 2110525
Dramamine Nausea Relief Pill SBDG · 2110526
Dramamine Nausea Relief BN · 2110522

📦 FDA Products & Package NDCs

1 product · 1 package NDC

1 package NDC map to RxCUI 2110527 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
63029-0905-10	2 BLISTER PACK in 1 BOX (63029-905-10) / 5 TABLET in 1 BLIS...	DRAMAMINE - N	Medtech Products Inc.	2018-01-15

Observed labelers: Medtech Products 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.