United States· US:49643-101_36ad1e17-751d-e226-e063-6394a90ab328
Alternaria
A alternaria alternata product containing alternaria alternata, registered in United States by Allermed Laboratories, Inc..
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
- ALTERNARIA ALTERNATA
- Manufacturer
- Allermed Laboratories, Inc.
- Country
- United States (US)
- ATC code
- Alternaria alternata
- ATC class
- Alternaria alternata
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 8
- ndc1149643-101-30
- ndc1149643101055 mL in 1 VIAL, MULTI-DOSE (49643-101-05)
- ndc11496431011010 mL in 1 VIAL, MULTI-DOSE (49643-101-10)
- ndc11496431013030 mL in 1 VIAL, MULTI-DOSE (49643-101-30)
- ndc11496431015050 mL in 1 VIAL, MULTI-DOSE (49643-101-50)
- ndc1149643-101-05
- ndc1149643-101-10
- ndc1149643-101-50
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Alternaria alternata in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandPrick-Test Alternaria alternata, PricktestlösungDermapharm AG
- GermanyAlk-Prick NAlk-Abelló Arzneimittel Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Germany · Alk-Prick N, Prick-Testlösung Alternaria Tenuis
- Denmark · Alk (Soluprick)
- Slovakia · Soluprick
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/6f954f24-0268-4e8d-96c0-897254fc1f3a GET /v1/drugs/6f954f24-0268-4e8d-96c0-897254fc1f3a?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": "ALTERNARIA ALTERNATA",
"productndc": "49643-101",
"dosage_form": "INJECTION",
"dea_schedule": null,
"strength_unit": "g/mL",
"application_number": "BLA102211",
"marketing_category": "BLA"
}See everything about alternaria alternata.
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.