United States· US:72162-1765_c4ae838c-25be-44fe-a54f-03495568e258
Diphenoxylate Hydrochloride and Atropine Sulfate
A medicinal product containing atropine sulfate; diphenoxylate hydrochloride, registered in United States by Bryant Ranch Prepack.
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
- ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
- Manufacturer
- Bryant Ranch Prepack
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- July 12, 2026
Packs & prices · 4
- ndc1172162176501000 TABLET in 1 BOTTLE (72162-1765-0)
- ndc117216217651100 TABLET in 1 BOTTLE (72162-1765-1)
- ndc1172162-1765-0
- ndc1172162-1765-1
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Atropine sulfate; diphenoxylate hydrochloride in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CanadaLOMOTILPFIZER CANADA ULC
- PolandReasecGedeon Richter Plc.
- CzechiaREASECGedeon Richter Plc., Budapešť
Authorised across Europe · EMA
The same active substance is authorised in 5 EEA countries. Names it is sold under:
- Cyprus · Lomotil
- Czechia · Reasec
- Hungary · Reasec
- Poland · Reasec
- Slovakia · Reasec
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/b2bd7e5d-8e75-423f-8336-66a6b208f6b0 GET /v1/drugs/b2bd7e5d-8e75-423f-8336-66a6b208f6b0?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": ".025; 2.5",
"substance": "ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE",
"productndc": "72162-1765",
"dosage_form": "TABLET",
"dea_schedule": "CV",
"strength_unit": "mg/1; mg/1",
"application_number": "ANDA086727",
"marketing_category": "ANDA"
}See everything about atropine sulfate; diphenoxylate 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.