United States· US:11822-0223_23afaba2-c43b-4295-8d40-7b81648fdcb1
acid reducer plus antacid
A medicinal product containing famotidine; calcium carbonate; magnesium hydroxide, registered in United States by Rite Aid Corporation.
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
- FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
- Manufacturer
- Rite Aid Corporation
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- July 26, 2026
Packs & prices · 2
- ndc1111822-0223-0
- ndc11118220223050 TABLET, CHEWABLE in 1 BOTTLE (11822-0223-0)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Famotidine; calcium carbonate; magnesium hydroxide in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- PolandManti ExtraUS Pharmacia Sp. z o.o.
- IrelandPepcid Duo Chewable Tablets Famotidine 10 mg Magnesium Hydroxide 165 mg Calcium Carbonate 800 mgJNTL Consumer Health (Ireland) Limited
- CanadaPEPCID COMPLETEMCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC
- SwedenPepcid Duo TuggtablettMcNeil Sweden AB
- NorwayPepcidduoMcNeil Sweden AB
- FinlandPepcid DuoMcNeil / JNTL Consumer Health (Finland) Oy
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Bulgaria · Гастропротект
- Finland · Pepcid Duo
- Ireland · Pepcid Duo
- Norway · Pepcidduo
- Poland · Manti Extra, Travisto Reflucontrol
- Sweden · Pepcid Duo
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/a0352d21-f42b-400f-9484-760e48351995 GET /v1/drugs/a0352d21-f42b-400f-9484-760e48351995?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": "800; 10; 165",
"substance": "FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE",
"productndc": "11822-0223",
"dosage_form": "TABLET, CHEWABLE",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1; mg/1",
"application_number": "ANDA077355",
"marketing_category": "ANDA"
}See everything about famotidine; calcium carbonate; magnesium hydroxide.
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.