United States· US:0268-0156_070eea8d-3fd1-452d-89de-1dbf1c19efb2
CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN
A medicinal product containing ambrosia artemisiifolia pollen, registered in United States by ALK-Abello, 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
- AMBROSIA ARTEMISIIFOLIA POLLEN
- Manufacturer
- ALK-Abello, Inc.
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- June 3, 2026
Packs & prices · 1
- ndc11026801563030 mL in 1 VIAL, MULTI-DOSE (0268-0156-30)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ambrosia artemisiifolia pollen in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Germany · Ragweed Prick Test Rx Roxall Medizin
- Hungary · Oraltek
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/7f20da3f-74f5-4308-93e0-0a2449749701 GET /v1/drugs/7f20da3f-74f5-4308-93e0-0a2449749701?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": "SUBCUTANEOUS",
"productid": "0268-0156_070eea8d-3fd1-452d-89de-1dbf1c19efb2",
"productndc": "0268-0156",
"dosage_form": "INJECTION, SUSPENSION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
"proprietary_name": "CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN",
"active_ingred_unit": "[PNU]/mL",
"application_number": "BLA103753",
"marketing_category": "BLA",
"nonproprietary_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
"start_marketing_date": "19750115",
"active_numerator_strength": "20000"
}See everything about ambrosia artemisiifolia pollen.
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.