United States· US:55910-943_596427a6-7028-4fed-b863-41686f3a81b0
Motion Sickness Relief
A medicinal product containing meclizine hydrochloride, registered in United States by DOLGENCORP, LLC.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- MECLIZINE HYDROCHLORIDE
- Manufacturer
- DOLGENCORP, LLC
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1155910943191 BLISTER PACK in 1 CARTON (55910-943-19) / 8 TABLET in 1 BLISTER PACK
- ndc1155910-943-19
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Meclizine hydrochloride in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandPostafenParanova Oy
- NorwayAgyrax2care4 ApS
- SpainNAVICALM 25 MG COMPRIMIDOSArafarma Group S.A.
- IcelandPostafenCampusPharma AB
- SwedenPostafen 25 mg TablettCampus Pharma AB
- BelgiumAgyrax 25 mgMediXal
- FranceAGYRAX, comprimé sécableMEDIXAL
- United KingdomSea-Legs 12.5mg tabletsG.R. Lane Health Products Ltd
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Belgium · Agyrax, Postafene
- Denmark · Postafen
- Spain · Chiclida
- Finland · Postafen
- France · Agyrax, Navidoxine
- United Kingdom (Northern Ireland) · Sea-Legs, Traveleeze
- Greece · Emetostop
- Iceland · Postafen
- Luxembourg · Agyrax, Postafene
- Netherlands · Suprimal
- Norway · Postafen
- Sweden · Postafen
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/da0398ff-e5ea-45f7-9dd8-15d04b385470 GET /v1/drugs/da0398ff-e5ea-45f7-9dd8-15d04b385470?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "ORAL",
"source": "ndc",
"strength": "25",
"substance": "MECLIZINE HYDROCHLORIDE",
"productndc": "55910-943",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "M009",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about meclizine hydrochloride.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.