United States· US:81284-831_7c1db393-3664-425f-af20-8d2175fb634e

ANTICHOLIUM

A medicinal product containing physostigmine salicylate, registered in United States by Provepharm Inc..

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…normalisedANTICHOLIUMATC—REGISTER NO.US:81284-831_7c1db393…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHYSOSTIGMINE SALICYLATE
Manufacturer
Provepharm Inc.
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

  • ndc11
    8128483105
    5 AMPULE in 1 CARTON (81284-831-05) / 5 mL in 1 AMPULE
  • ndc11
    81284-831-05

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Physostigmine salicylate in 3 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All physostigmine salicylate products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Austria · Anticholium
  • Germany · Anticholium

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/9b6efbf1-982f-40c7-8f2f-3743f0022e36
GET /v1/drugs/9b6efbf1-982f-40c7-8f2f-3743f0022e36?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": "INTRAVENOUS",
  "source": "ndc",
  "strength": ".4",
  "substance": "PHYSOSTIGMINE SALICYLATE",
  "productndc": "81284-831",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE"
}

See everything about physostigmine salicylate.

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.