United States· US:49643-015_36ad1e17-751d-e226-e063-6394a90ab328

Horse Epithelia

A medicinal product containing equus caballus skin, registered in United States by Allermed Laboratories, Inc..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedHorse EpitheliaATC—REGISTER NO.US:49643-015_36ad1e17…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
EQUUS CABALLUS SKIN
Manufacturer
Allermed Laboratories, 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 · 8

  • ndc11
    49643-015-30
  • ndc11
    49643-015-05
  • ndc11
    49643-015-50
  • ndc11
    49643-015-10
  • ndc11
    4964301505
    5 mL in 1 VIAL, MULTI-DOSE (49643-015-05)
  • ndc11
    4964301510
    10 mL in 1 VIAL, MULTI-DOSE (49643-015-10)
  • ndc11
    4964301530
    30 mL in 1 VIAL, MULTI-DOSE (49643-015-30)
  • ndc11
    4964301550
    50 mL in 1 VIAL, MULTI-DOSE (49643-015-50)

Regulatory notes

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

Same medicine, other countries

Equus caballus skin in 1 other country

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

All equus caballus skin products

Authorised across Europe · EMA

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

  • Germany · Prick-Testlösung Pferdeepithelien, Provokations-Testlösung Pferdeepithelien
  • Hungary · Alyostal Prick Állati Eredetű Allergének

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/ea9534ff-115d-45c9-b5d1-7e371b06ccb9
GET /v1/drugs/ea9534ff-115d-45c9-b5d1-7e371b06ccb9?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": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "source": "ndc",
  "strength": ".1",
  "substance": "EQUUS CABALLUS SKIN",
  "productndc": "49643-015",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA"
}

See everything about equus caballus skin.

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.