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United States· US:36800-616_2ebdee8c-703f-4a75-a79a-b908ce54f30d

topcare dual action complete

A medicinal product containing famotidine; calcium carbonate; magnesium hydroxide, registered in United States by Topco Associates LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedtopcare dual action completeATC—REGISTER NO.US:36800-616_2ebdee8c…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Manufacturer
Topco Associates 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 · 4

  • ndc11
    3680061663
    25 TABLET, CHEWABLE in 1 BOTTLE (36800-616-63)
  • ndc11
    3680061671
    50 TABLET, CHEWABLE in 1 BOTTLE (36800-616-71)
  • ndc11
    36800-616-63
  • ndc11
    36800-616-71

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.

All famotidine; calcium carbonate; magnesium hydroxide products

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/baae0269-dd9e-4e44-9249-4bf111a567a8
GET /v1/drugs/baae0269-dd9e-4e44-9249-4bf111a567a8?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": "10; 800; 165",
  "substance": "FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE",
  "productndc": "36800-616",
  "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.